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

Name: FDA 510(k) clearance K791888
Creator: U.S. Food and Drug Administration
Published: 1979-10-17

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.. Device class: Unclassified.

Clearance details

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

Download summary PDF View on FDA.gov ↗

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K990584 — GAUZE SPONGES: LAPAROTOMY SPONGE, X-RAY DETECTABLE1999-04-23
K984187 — CROSSTEX NON-WOVEN SPONGES1999-02-18

More clearances from Ascep, Inc.

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K830219 — VARIOUS INSTRUMENTS & INSTRUMENT TRAYS1983-04-12
K822893 — G.E.V. DISPOSABLE SCALPELS1982-10-22
K810004 — STERILE DISPOSABLE INSTRUMENT TRAYS1981-01-26
K802726 — INSTRUMENTS NONSTERILE & STERILE1980-11-19
K791886 — I.V. CARE KIT1979-10-26

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