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

Cameron-Miller, Inc. — Predicate Candidate Screening

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

88 daysmedian FDA review time
429 days90th percentile
14clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K944775ELECTROSURGICAL UNIT MODEL 26-0335Cameron-Miller, Inc.1994-10-11140
K931541MODEL 26-0375, ELECTROSURGICAL GENERATORCameron-Miller, Inc.1994-06-014290
K931437MODEL 80-1983, ELECTROSURGICAL GENERATORCameron-Miller, Inc.1994-05-274310
K935490ELECTROSURGICAL DEVICE, MODEL 26-2500Cameron-Miller, Inc.1994-04-011370
K854109ELECTROSURGICAL DEVICES, 26-0330,26-335,340 & 0345Cameron-Miller, Inc.1986-01-241080
K853972CAMERON-MILLER MODEL 80-2701, BIPOLAR COAGULATORCameron-Miller, Inc.1986-01-241200
K833449HAND CONTROLLED PENCIL OR SWITCH HANDCameron-Miller, Inc.1983-11-29550
K822092CAMERON-MILLER #40-1516Cameron-Miller, Inc.1982-09-21670
K812702TECHNICATORCameron-Miller, Inc.1981-11-05430
K791415MODEL 80-1765 ELECTROSURGICAL UNITCameron-Miller, Inc.1979-10-11720
K781353PAPILLOTOME CUTTING SNARECameron-Miller, Inc.1978-10-10640
K780433FIBER OPTIC ADJUSTABLE HEADLIGHTCameron-Miller, Inc.1978-06-13880
K772235HAND CONTROL ACCESS.-ELECTROSURG. UNITSCameron-Miller, Inc.1977-12-1360
K771639ELECTROSURGICAL GENERATORCameron-Miller, Inc.1977-11-29950

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