HEMOCLIP LIGATING CLIPS M/LARGE
K-Number: K841548 · 1984-08-14
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Device Summary
Frequently Asked Questions
What is the HEMOCLIP LIGATING CLIPS M/LARGE?
HEMOCLIP LIGATING CLIPS M/LARGE is a medical device that received FDA 510(k) clearance on 1984-08-14. The listed applicant is Edward Weck, Inc.. The 510(k) number is K841548.
When did HEMOCLIP LIGATING CLIPS M/LARGE receive FDA 510(k) clearance?
HEMOCLIP LIGATING CLIPS M/LARGE received FDA 510(k) clearance on 1984-08-14, under 510(k) number K841548.
Who is the listed applicant for HEMOCLIP LIGATING CLIPS M/LARGE?
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 LIGATING CLIPS M/LARGE?
The FDA product code for HEMOCLIP LIGATING CLIPS M/LARGE 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.
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