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

QUANTUM 3080 SURGICAL TABLE

K Number: K930493 · Decision Jun 22, 1993
Classifications
1
FEI Numbers
73
Registration Numbers
73
Same Product Code
34
Applicant Total
36
Review Days
141

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
QUANTUM 3080 SURGICAL TABLE
K Number
K930493
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4960
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
American Sterilizer Co.
Date Received
February 1, 1993
Decision Date
June 22, 1993
Product Code
FQO
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
FQO Table, Operating-Room, Ac-Powered

Similar 510(k) Clearances

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

View all

Other Clearances by American Sterilizer Co.

K Number Device Name
K943288 AMSCO SQ240 SURGICAL LIGHT
K931872 THE EAGLE 3017 100% ETHYLENE OXIDE STERILIZER
K922485 CHEMDI-VHP CHEMICAL INDICATOR
K905816 ORTHOVISION TABLE
K896674 AMSCO QUANTUM LIGHT
K895164 EAGLE DS
K882660 GENERAL SURGICAL TABLE AND ACCESSORIES
K880198 GEMINI SURGICAL LIGHT
K864846 RADIOGRAPHIC - LEG SECTION
K844479 CHEMSPOR
Search all 36 clearances from American Sterilizer Co. →