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

DEVMED LENS WASH SHEATH

K Number: K925669 · Decision Feb 23, 1993
Classifications
1
FEI Numbers
548
Registration Numbers
548
Same Product Code
1422
Applicant Total
3
Review Days
105

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Basic Information

Device Name
DEVMED LENS WASH SHEATH
K Number
K925669
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Devmed Corp.
Date Received
November 10, 1992
Decision Date
February 23, 1993
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 Devmed Corp.

K Number Device Name
K972152 DEVMED STEPPING AND STABILIZING SYSTEM
K933416 DEVMED LAP WASH REUSABLE ENDOSCOPIC LENS WASH SHEATH