CATHETER CARE KIT REORDER 7940&7941
K-Number: K791888 · 1979-10-17
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Device Summary
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.
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
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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