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Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Dahlberg Electronics, Inc. — Predicate Candidate Screening

31 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

29 daysmedian FDA review time
90 days90th percentile
31clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K896157DAHLBERG MODEL LH BEHIND-THE-EAR HEARING AIDDahlberg Electronics, Inc.1990-01-22900
K896159DAHLBERG MODEL LP BEHIND-THE-EAR HEARING AIDDahlberg Electronics, Inc.1990-01-22900
K896158DAHLBERG MODEL LA BEHIND-THE-EAR HEARING AIDDahlberg Electronics, Inc.1990-01-22900
K881417DAHLBERG MODEL GP BODY AIDDahlberg Electronics, Inc.1988-06-07640
K881612DAHLBERG MODEL XJ 8080 BODY-WORN HEARING AIDDahlberg Electronics, Inc.1988-06-01500
K874831AUDIOTONE MODEL A2000 BEHIND-THE-EAR HEARING AIDDahlberg Electronics, Inc.1988-02-22900
K874830MIRACLE EAR MODEL BP BEHIND-THE-EAR HEARING AIDDahlberg Electronics, Inc.1988-02-17850
K873169DAHLBERG MODEL GH BODY AIDDahlberg Electronics, Inc.1987-09-16360
K873397DAHLBERG MODEL MH BEHIND-THE-EAR HEARING AIDDahlberg Electronics, Inc.1987-09-14210
K873376MODEL SI AND SP BEHIND-THE-EAR HEARING AIDDahlberg Electronics, Inc.1987-09-14210
K871525DAHLBERG MODEL UL IN-THE-EAR HEARING AIDDahlberg Electronics, Inc.1987-05-19290
K871524DAHLBERG MODEL UH IN-THE-EAR HEARING AIDDahlberg Electronics, Inc.1987-05-08180
K870691DAHLBERG MODEL UV TRIMLINE IN-THE-EAR HEARING AIDDahlberg Electronics, Inc.1987-03-13220
K860670DAHLBERG MODEL UT IN-THE-EAR HEARING AIDDahlberg Electronics, Inc.1986-04-11460
K850980CRESTLINE CL IN-THE-EAR HEARING AIDDahlberg Electronics, Inc.1985-06-191000
K850981CRESTLINE CB BEHIND-THE-EAR HEARING AIDDahlberg Electronics, Inc.1985-05-31810
K833073DAHLBERG #USS IN THE EAR HEARING AIDDahlberg Electronics, Inc.1983-10-28490
K821550MODEL AH BEHING-THE-EAR-HEARING AIDDahlberg Electronics, Inc.1982-06-14200
K820398DAHLBERG HEARING AID MODEL ALDahlberg Electronics, Inc.1982-03-02190
K811578DAHLBERG MODEL AP HEARING AIDDahlberg Electronics, Inc.1981-07-01260
K811226DAHLBERG MODEL AMDahlberg Electronics, Inc.1981-05-1390
K802510DAHLBERG HEARING AID MODEL AIDahlberg Electronics, Inc.1980-10-2380
K801115DAHLBERG HEARING AID MODEL MELDahlberg Electronics, Inc.1980-05-28160
K801114DAHLBERG HEARING AID MODEL MEHDahlberg Electronics, Inc.1980-05-28160
K800571DAHLBERG #AZ BEHIND THE EAR HEARING AIDDahlberg Electronics, Inc.1980-03-2060
K800181DAHLBERG # AF BEHING THE EAR HEARING/AIDDahlberg Electronics, Inc.1980-02-28300
K792278DAHLBERG MODEL AE HIGH FREQUENCY / AIDDahlberg Electronics, Inc.1979-11-30170
K791310DAHLBERG HEARING AID MODEL GCDahlberg Electronics, Inc.1979-09-28740
K791311DAHLBERG HEARING AID MODEL UNDahlberg Electronics, Inc.1979-09-19650
K782121HEARING AID, MODEL GBDahlberg Electronics, Inc.1979-01-22260
K782122HEARING AID, MODEL AADahlberg Electronics, Inc.1979-01-22260

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda