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

ELEVATOR CUSHION

K Number: K832472 · Decision Sep 20, 1983
Classifications
1
FEI Numbers
162
Registration Numbers
162
Same Product Code
60
Applicant Total
32
Review Days
56

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
ELEVATOR CUSHION
K Number
K832472
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4950
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Inmed Corp.
Date Received
July 26, 1983
Decision Date
September 20, 1983
Product Code
FWZ
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
FWZ Operating Room Accessories Table Tray

Similar 510(k) Clearances

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

View all

Other Clearances by Inmed Corp.

K Number Device Name
K862672 ESOPHAGEAL STETHOSCOPE WITH THERMISTOR
K853162 STERILE NASOPHARYNGEAL AIRWAY
K850152 PRECONNECTED URETHRAL CATHETER TRAY
K850335 URETEROSCOPY CATHETER
K850248 DISPOSABLE GUEDEL AIRWAY
K844801 ULTRA EXTERNAL CATHETER
K842301 DISPOSABLE LATEX BANDAGE
K842866 URETHRAL CATHETERIZATION TRAY
K841040 FOX POST NASAL BALLOON CATHETER
K842865 ESOPHAGEAL STETHOSCOPE
Search all 32 clearances from Inmed Corp. →