Atlas FDA

FLOWCLAMP CAT.#1011 & 1012

FDA 510(k) clearance K802009 · decided 1980-10-31

Clearance details

K-number
K802009
Device name
FLOWCLAMP CAT.#1011 & 1012
Applicant
Pollak (Intl.), Ltd.
Decision
Substantially Equivalent
Date received
1980-08-20
Decision date
1980-10-31
Days to decision
72 days
Clearance type
Traditional
Product code
FKK
Device class
1
Regulation number
876.4730
Medical specialty
Gastroenterology, Urology
Advisory committee
Gastroenterology, Urology
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
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
AMP CAPD UNISPIKE AMINISTRATION SET (K822551)American Medical Products, Inc.1982-10-13

Recalls involving this device

No recalls on record reference this clearance.