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

H. PYLORI QUIK CHEK

K Number: K181379 · Decision Aug 21, 2018
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
90
Applicant Total
36
Review Days
89

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Basic Information

Device Name
H. PYLORI QUIK CHEK
K Number
K181379
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.3110
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Techlab, Inc.
Date Received
May 24, 2018
Decision Date
August 21, 2018
Product Code
LYR
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
LYR Helicobacter Pylori

Similar 510(k) Clearances

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

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Other Clearances by Techlab, Inc.

K Number Device Name
K191442 Campylobacter Chek
K191456 Campylobacter Quik Chek
K181400 H. PYLORI 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. →