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

SHUR-GRIP

K Number: K912834 · Decision Jul 26, 1991
Classifications
1
FEI Numbers
231
Registration Numbers
231
Same Product Code
66
Applicant Total
14
Review Days
30

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Basic Information

Device Name
SHUR-GRIP
K Number
K912834
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Inman Medical Corp.
Date Received
June 26, 1991
Decision Date
July 26, 1991
Product Code
KDC
Advisory Committee
General, Plastic Surgery
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
KDC Instrument, Surgical, Disposable

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Other Clearances by Inman Medical Corp.

K Number Device Name
K933171 INMAN IRRIGATION TAPERED PROBE
K933169 INMAN ENDOSCOPIC BLUNT DISSECTOR
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
Search all 14 clearances from Inman Medical Corp. →