CATHETER CARE KIT REORDER 7940&7941— 510(k) K791888

Substantially Equivalent

Ascep, Inc.

FDA 510(k) clearance K791888 for CATHETER CARE KIT REORDER 7940&7941, Substantially Equivalent on 1979-10-17. Applicant: Ascep, Inc..

Clearance details

Applicant: Ascep, Inc.
Product code: Code EFQ
Advisory panel: Unknown
Date received: 1979-09-11
Decision date: 1979-10-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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