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

SKYTRON MODEL 130 SURGICAL TABLE

K Number: K873478 · Decision Sep 24, 1987
Classifications
1
FEI Numbers
6
Registration Numbers
6
Same Product Code
3
Applicant Total
19
Review Days
31

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
SKYTRON MODEL 130 SURGICAL TABLE
K Number
K873478
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4950
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Skytron, Div. the Kmw Group, Inc.
Date Received
August 24, 1987
Decision Date
September 24, 1987
Product Code
FWY
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
FWY Table, Operating-Room, Non-Electrical

Similar 510(k) Clearances

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

View all

Other Clearances by Skytron, Div. the Kmw Group, Inc.

K Number Device Name
K071698 AURORA LED SERIES SURGICAL LIGHTS
K021585 STELLAR SERIES SURGICAL LIGHTS WITH HERMES
K002463 STELLAR
K992090 MILLENNIUM GOLD
K950192 SKYTRON SKYBOOM SERIES
K940616 SKYTRON ELITE 3500 TABLE
K933564 SKYTRON EXAM LIGHT
K926045 SKYTRON LIFE ISLAND 21
K915285 SKYTRON INFINITY SERIES SURGICAL LIGHTS
K900472 SKYTRON MODEL 860 AND 800 COMP. SURGITA NEURO EQUI
Search all 19 clearances from Skytron, Div. the Kmw Group, Inc. →