Atlas FDA

BIOTEL (TM)/UTI

FDA 510(k) clearance K855238 · decided 1986-05-09

Clearance details

K-number
K855238
Device name
BIOTEL (TM)/UTI
Applicant
American Diagnostic Corp.
Decision
Substantially Equivalent
Date received
1985-12-31
Decision date
1986-05-09
Days to decision
129 days
Clearance type
Traditional
Product code
JMT
Device class
1
Regulation number
862.1510
Medical specialty
Clinical Chemistry
Advisory committee
Clinical Chemistry
Location
Wheaton, IL, US
Third-party review
No
Expedited review
No

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DBEST URINARY TRACT INFECTION TEST KIT FOR HOME-USE (K990873)Ameritek, Inc.1999-09-01
URITEST - NITRITE IN URINE TEST (K954685)Tcpi, Inc.1996-07-22
CHEK-STIX U.T.I. SELF-TEST (K960888)Bayer Corp.1996-07-05
FIRST CHOICE URINARY TRACT INFECTION TEST STRIPS (K953672)Polymer Technology Intl.1996-07-01
BIOSCAN URINE DIAGNOSTIC REAGENT STRIPS (K875248)Bioscan Instruments, Inc.1988-02-24
KYOTEST 8V (K840828)Kyoto Diagnostics, Inc.1984-05-14

Recalls involving this device

No recalls on record reference this clearance.