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

BIOSIGN H. PYLORI WB-NEW ONE-STEP ANTI-H. PYLORI ANTIBODY TEST

K Number: K980798 · Decision Sep 22, 1998
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
90
Applicant Total
72
Review Days
204

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
BIOSIGN H. PYLORI WB-NEW ONE-STEP ANTI-H. PYLORI ANTIBODY TEST
K Number
K980798
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.3110
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Princeton BioMeditech Corp.
Date Received
March 2, 1998
Decision Date
September 22, 1998
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.

View all

Other Clearances by Princeton BioMeditech Corp.

K Number Device Name
K251538 Status™ COVID-19/Flu A&B
K182157 BioSign Flu A+B
K130650 STATUS DS OXY
K133474 BIOSIGN FLU A + B, STATUS FLU A & B
K132465 BIOSIGN FLU A + B, STATUS FLU A & B
K083746 BIOSIGN FLU A+B
K100817 BIOSIGN IFOBTEST, BIOSIGN FECAL OCCULT BLOOD TEST
K100341 SPERMCHECK FERTILITY
K082661 BIOSTREP A, BIOSIGN STREP A, STATUSFIRST STREP A
K073039 SPERMCHECK VASECTOMY
Search all 72 clearances from Princeton BioMeditech Corp. →