FDA 510(k) FDA class 2 Unknown 🇺🇸 United States

MIC (SPECIFIC LINE) INSERTION KIT

K Number: K875126 · Decision Mar 2, 1988
Classifications
1
FEI Numbers
228
Registration Numbers
229
Same Product Code
648
Applicant Total
24
Review Days
78

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
MIC (SPECIFIC LINE) INSERTION KIT
K Number
K875126
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5980
Medical Specialty
Gastroenterology, Urology
Decision
Unknown
Applicant
Medical Innovations Corp.
Date Received
December 15, 1987
Decision Date
March 2, 1988
Product Code
KNT
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
KNT Tubes, Gastrointestinal (And Accessories)

Similar 510(k) Clearances

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

View all

Other Clearances by Medical Innovations Corp.

K Number Device Name
K945612 MIC NASOGASTRIC-GASTROJEJUNAL FEEDING TUBE
K940548 MIC PERCUTANEOUS ENDOSCOPIC JEJUNAL FEEDING TUBE
K943685 MIC DISPOSABLE SNARE
K926581 MIC TRANSGASTRIC JEJUNAL TUBE
K921652 MIC TRANSGASTRIC JEJUNAL FEEDING TUBE KIT
K921370 MIC GASTRO-ENTEROSTOMY TUBE MODIFICATION
K924065 MIC PEG TUBE
K922667 MIC LOW PROFILE GASTROSTOMY TUBE
K913320 MIL CM-II COAGULATION MACHINE
K903531 ANTICARDIOLIPIN ANTIBODY TEST SYSTEM
Search all 24 clearances from Medical Innovations Corp. →