FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

GENYX MEDICAL INJECTION NEEDLE

K Number: K990996 · Decision Jun 18, 1999
Classifications
1
FEI Numbers
98
Registration Numbers
98
Same Product Code
88
Applicant Total
1
Review Days
85

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
GENYX MEDICAL INJECTION NEEDLE
K Number
K990996
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Genyx Medical, Inc.
Date Received
March 25, 1999
Decision Date
June 18, 1999
Product Code
FBK
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
FBK Endoscopic Injection Needle, Gastroenterology-Urology

Similar 510(k) Clearances

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

View all