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FDA 510(k)

CEPTI-SEAL DRESSING CHNG. KIT FOR CENT. VENOUS CAT

K-Number: K920398 · 1992-04-15

ApplicantMedi-Flex Hospital Products, Inc.
Decision Date1992-04-15
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CEPTI-SEAL DRESSING CHNG. KIT FOR CENT. VENOUS CAT is the device name listed in this FDA 510(k) record. The listed applicant is Medi-Flex Hospital Products, Inc.. It received FDA 510(k) clearance on 1992-04-15 under 510(k) number K920398. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CEPTI-SEAL DRESSING CHNG. KIT FOR CENT. VENOUS CAT?

CEPTI-SEAL DRESSING CHNG. KIT FOR CENT. VENOUS CAT is a medical device that received FDA 510(k) clearance on 1992-04-15. The listed applicant is Medi-Flex Hospital Products, Inc.. The 510(k) number is K920398.

When did CEPTI-SEAL DRESSING CHNG. KIT FOR CENT. VENOUS CAT receive FDA 510(k) clearance?

CEPTI-SEAL DRESSING CHNG. KIT FOR CENT. VENOUS CAT received FDA 510(k) clearance on 1992-04-15, under 510(k) number K920398.

Who is the listed applicant for CEPTI-SEAL DRESSING CHNG. KIT FOR CENT. VENOUS CAT?

The FDA 510(k) record lists Medi-Flex Hospital Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CEPTI-SEAL DRESSING CHNG. KIT FOR CENT. VENOUS CAT?

The FDA product code for CEPTI-SEAL DRESSING CHNG. KIT FOR CENT. VENOUS CAT is FMF.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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