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

INMAN ENDOSCOPIC BLUNT DISSECTOR

K Number: K933169 · Decision Apr 19, 1994
Classifications
1
FEI Numbers
548
Registration Numbers
548
Same Product Code
1422
Applicant Total
14
Review Days
294

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Basic Information

Device Name
INMAN ENDOSCOPIC BLUNT DISSECTOR
K Number
K933169
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Inman Medical Corp.
Date Received
June 29, 1993
Decision Date
April 19, 1994
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.

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Other Clearances by Inman Medical Corp.

K Number Device Name
K933171 INMAN IRRIGATION TAPERED PROBE
K933094 INSUFFLATOR TUBING KIT W/FILTER
K933382 IMC CABLE/WIRE COVER
K933774 IMC SALINE WET DRESSING
K933305 IMC 5.0MM IRRIGATION/ASPIRATION PROBE
K933306 IMC 5.0MM IRRIGATION/ASPIRATION PROBE W/HOLES
K933170 INMAN POOLE TIP SUCTION PROBE W/TUBING KIT
K932762 10.0MM SUCTION/IRRIGATION PROBE & TUBING KIT
K933371 IMC ENDOSCOPIC INSTRUMENT HOLDER
K921291 INMAN MEDICAL PACKING STRIP
Search all 14 clearances from Inman Medical Corp. →