FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

OSOM HCG COMBO TEST

K Number: K955141 · Decision Dec 6, 1995
Classifications
1
FEI Numbers
269
Registration Numbers
269
Same Product Code
492
Applicant Total
12
Review Days
23

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Basic Information

Device Name
OSOM HCG COMBO TEST
K Number
K955141
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1660
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Wyntek Diagnostics, Inc.
Date Received
November 13, 1995
Decision Date
December 6, 1995
Product Code
JJX
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JJX Single (Specified) Analyte Controls (Assayed And Unassayed)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JJX), ordered by most recent decision date.

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Other Clearances by Wyntek Diagnostics, Inc.

K Number Device Name
K992658 OSOM ULTRA STREP A TEST, MODEL 147
K990578 OSOM CARD II HCG-URINE TEST, MODEL 102
K990576 OSOM CARD PREGNANCY TEST, MODEL 103
K974159 OSOM HCG-URINE TEST MODEL 101
K973879 OSOM CARD HCG-URINE TEST
K972231 OSOM MONO TEST 143
K965227 OSOM CLASSIC HCG-URINE TEST (115)
K965184 PERFECTA PREGNANCY TEST
K961423 OSOM STREP A TEST
K954178 OSOM PREGNANCY TEST
Search all 12 clearances from Wyntek Diagnostics, Inc. →