VEIN CLAMPS
K-Number: K772137 · 1977-11-21
Advertisement
Device Summary
Frequently Asked Questions
What is the VEIN CLAMPS?
VEIN CLAMPS is a medical device that received FDA 510(k) clearance on 1977-11-21. The listed applicant is A&A Ent.. The 510(k) number is K772137.
When did VEIN CLAMPS receive FDA 510(k) clearance?
VEIN CLAMPS received FDA 510(k) clearance on 1977-11-21, under 510(k) number K772137.
Who is the listed applicant for VEIN CLAMPS?
The FDA 510(k) record lists A&A Ent. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VEIN CLAMPS?
The FDA product code for VEIN CLAMPS is DXC.
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 A&A Ent. 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: DXC)
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.
Advertisement