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

Campylobacter Quik Chek

K Number: K191456 · Decision Jun 20, 2019
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
11
Applicant Total
36
Review Days
20

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Basic Information

Device Name
Campylobacter Quik Chek
K Number
K191456
Device Class
FDA class 1
Clearance Type
Special
Regulation Number
866.3110
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Techlab, Inc.
Date Received
May 31, 2019
Decision Date
June 20, 2019
Product Code
LQP
Advisory Committee
Microbiology
Review Advisory Committee
MI
Third Party
N

Classifications

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

Product Code Device Name
LQP Campylobacter Spp.

Similar 510(k) Clearances

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

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Other Clearances by Techlab, Inc.

K Number Device Name
K191442 Campylobacter Chek
K181400 H. PYLORI CHEK™
K181379 H. PYLORI QUIK CHEK
K173217 CAMPYLOBACTER QUIK CHEK
K173219 CAMPYLOBACTER CHEK
K171078 TRI-COMBO PARASITE SCREEN
K170728 E. HISTOLYTICA QUIK CHEK
K082499 C. DIFF QUIK CHEK COMPLETE
K053572 C. DIFF QUIK CHEK
K051927 TECHLAB ASCA-CHEK
Search all 36 clearances from Techlab, Inc. →