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

ENDOSCOPIC BLUNT DISSECTING INSTRUMENT

K Number: K931854 · Decision Aug 10, 1993
Classifications
1
FEI Numbers
3
Registration Numbers
3
Same Product Code
3
Applicant Total
10
Review Days
119

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Basic Information

Device Name
ENDOSCOPIC BLUNT DISSECTING INSTRUMENT
K Number
K931854
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Mayaguez Medical Center
Date Received
April 13, 1993
Decision Date
August 10, 1993
Product Code
FGS
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
FGS Carrier, Sponge, Endoscopic

Similar 510(k) Clearances

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

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Other Clearances by Mayaguez Medical Center

K Number Device Name
K932804 IRRIGATING TAPERED PROBE
K932805 10.0MM SUCTION/IRRIGATION PROBE & TUBING KIT
K931950 POOLE TIP SUCTION PROBE
K932806 POOLE TIP SUCTION PROBE & TUBING KIT
K931856 5.0 MM IRRIGATION/ASPIRATION PROBE
K931912 IRRIGATING BLUNT DISSECTOR
K931707 ENDOSCOPIC CABLE/WIRE COVER
K931706 ENDOSCOPIC CABLE DRAPE
K931705 ENDOSCOPIC INSTRUMENT HOLDER