Atlas FDA

SUPPORT PRODUCTS EXAMPLE PROSET CAST

FDA 510(k) clearance K830650 · decided 1983-07-07

Clearance details

K-number
K830650
Device name
SUPPORT PRODUCTS EXAMPLE PROSET CAST
Applicant
Isopedix Corp.
Decision
Substantially Equivalent
Date received
1983-03-03
Decision date
1983-07-07
Days to decision
126 days
Clearance type
Traditional
Product code
ITG
Device class
1
Regulation number
890.3025
Medical specialty
Physical Medicine
Advisory committee
Physical Medicine
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
CONFORMA(TM) PLASTER BANDAGES (K873111)The Kendal Co.1987-10-09
DEKNA BAND KIT (K862115)Deknatel, Inc.1986-08-19
T.P.G. CAST TAPE (K842573)The Poly Group, Inc.1984-08-10
HEXCELITE (K840416)Hexcel Medical1984-03-23
NON WETTING UNDERCAST PADDING (K833732)American Medical Disposable, Inc.1983-12-12
SOFFBAN ORTHOPEDIC PADDING (K832992)Smith & Nephew, Inc.1983-11-14
ORTHOPEDIC CASTING TAPE MAXCAST (K832237)Cutter Laboratories, Inc.1983-08-16
YESONA PLASTER OF PARIS BANDAGE (K831492)Watson Phillips Y Cia. Sucs., S.A. DE C.V.1983-06-30
URETHANE ORTHOPAEDIC CASTING TAPE (K820890)Hexcel Medical1982-06-23
WEBRIL CAST PADDING (K820140)Stan-Pak Ent.1982-02-12
SPECIALIST CAST PADDING (K820155)Stan-Pak Ent.1982-02-12
ULTRACAST WATERLESS SYNTHETIC RESIN CAST (K813052)Zimmer, Inc.1982-02-04

Recalls involving this device

No recalls on record reference this clearance.