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

INTRODUCER

K Number: K951090 · Decision Jul 11, 1995
Classifications
1
FEI Numbers
548
Registration Numbers
548
Same Product Code
1422
Applicant Total
12
Review Days
124

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
INTRODUCER
K Number
K951090
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Ranfac, Corp.
Date Received
March 9, 1995
Decision Date
July 11, 1995
Product Code
GCJ
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
GCJ Laparoscope, General & Plastic Surgery

Similar 510(k) Clearances

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

View all

Other Clearances by Ranfac, Corp.

K Number Device Name
K162932 Ranfac Fat Aspiration Cannula
K150156 Ranfac Fat Aspiration Transfer Syringe (FATS) Procedure Pack, Ranfac Fat Aspiration Transfer Syringe (FATS) Containment Vessel
K150563 Marrow Cellution Bone Marrow Aspiration Needle
K140991 RANFAC ASPIRATION NEEDLE WITH ADJUSTABLE GUIDE
K131157 RANFAC BONE MARROW ASPIRATION NEEDLE
K031344 RANFAC GOLDENBERG SNARECOIL SOFT TISSUE BIOPSY (GSS) NEEDLE
K012224 SINGLE ACTION BIOPSY NEEDLE, MODEL RCBS: XX GAUGE, XX LENGTH, XX THROW
K961922 RDP-2
K930474 NEEDLE, PNEUMOPERITONEUM, SPRING LOADED
K864139 RANFAC CUT BIOPSY NEEDLE
Search all 12 clearances from Ranfac, Corp. →