Atlas FDA

AMP CAPD UNISPIKE AMINISTRATION SET

FDA 510(k) clearance K822551 · decided 1982-10-13

Clearance details

K-number
K822551
Device name
AMP CAPD UNISPIKE AMINISTRATION SET
Applicant
American Medical Products, Inc.
Decision
Substantially Equivalent
Date received
1982-08-24
Decision date
1982-10-13
Days to decision
50 days
Clearance type
Traditional
Product code
FKK
Device class
1
Regulation number
876.4730
Medical specialty
Gastroenterology, Urology
Advisory committee
Gastroenterology, Urology
Location
Freehold, NJ, 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
TUBING CLAMP CAT#1000-A (K854512)Rao Medical Devices, Inc.1985-12-02
NEW TRAVENOL ROLLER CLAMP-SOLUTION ADMIN. SET (K854517)Travenol Laboratories, S.A.1985-12-02
CLAMP, TUBING, LINE (K844121)Dyn-A-Med Products1984-12-17
EMPTY DIALYSATE CONTAINER (K831689)Delmed, Inc.1983-08-11
FLOWCLAMP CAT.#1011 & 1012 (K802009)Pollak (Intl.), Ltd.1980-10-31

Recalls involving this device

No recalls on record reference this clearance.