IMPRA DUAL LUMEN SUBCLAVIAN - FEMORAL CATHETER— 510(k) K883592

Unknown

Impra, Inc.

FDA 510(k) clearance K883592 for IMPRA DUAL LUMEN SUBCLAVIAN - FEMORAL CATHETER, Unknown on 1988-12-08. Applicant: Impra, Inc..

Clearance details

Applicant: Impra, Inc.
Product code: Code LFJ
Advisory panel: Gastroenterology, Urology
Date received: 1988-08-23
Decision date: 1988-12-08
Decision: Unknown
Clearance type: Traditional
Location: Tempe, AZ, US

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