HEMOCLIP SURGICAL OCCLUDING CLIP
K-Number: K800079 · 1980-01-28
Advertisement
Device Summary
Frequently Asked Questions
What is the HEMOCLIP SURGICAL OCCLUDING CLIP?
HEMOCLIP SURGICAL OCCLUDING CLIP is a medical device that received FDA 510(k) clearance on 1980-01-28. The listed applicant is Edward Weck, Inc.. The 510(k) number is K800079.
When did HEMOCLIP SURGICAL OCCLUDING CLIP receive FDA 510(k) clearance?
HEMOCLIP SURGICAL OCCLUDING CLIP received FDA 510(k) clearance on 1980-01-28, under 510(k) number K800079.
Who is the listed applicant for HEMOCLIP SURGICAL OCCLUDING CLIP?
The FDA 510(k) record lists Edward Weck, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HEMOCLIP SURGICAL OCCLUDING CLIP?
The FDA product code for HEMOCLIP SURGICAL OCCLUDING CLIP is FZP.
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 Edward Weck, 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: FZP)
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