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FDA 510(k)

CATHETER CARE KIT REORDER 7940&7941

K-Number: K791888 · 1979-10-17

ApplicantAscep, Inc.
Decision Date1979-10-17
Product CodeEFQ
DecisionSubstantially Equivalent

Device Summary

CATHETER CARE KIT REORDER 7940&7941 is the device name listed in this FDA 510(k) record. The listed applicant is Ascep, Inc.. It received FDA 510(k) clearance on 1979-10-17 under 510(k) number K791888. The device is classified under product code EFQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CATHETER CARE KIT REORDER 7940&7941?

CATHETER CARE KIT REORDER 7940&7941 is a medical device that received FDA 510(k) clearance on 1979-10-17. The listed applicant is Ascep, Inc.. The 510(k) number is K791888.

When did CATHETER CARE KIT REORDER 7940&7941 receive FDA 510(k) clearance?

CATHETER CARE KIT REORDER 7940&7941 received FDA 510(k) clearance on 1979-10-17, under 510(k) number K791888.

Who is the listed applicant for CATHETER CARE KIT REORDER 7940&7941?

The FDA 510(k) record lists Ascep, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CATHETER CARE KIT REORDER 7940&7941?

The FDA product code for CATHETER CARE KIT REORDER 7940&7941 is EFQ.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Ascep, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 9 devices →

Related Devices (Code: EFQ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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

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