HEMOCLIP AUTOMATIC CLIPS MEDIUM
K-Number: K841549 · 1984-08-14
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Device Summary
Frequently Asked Questions
What is the HEMOCLIP AUTOMATIC CLIPS MEDIUM?
HEMOCLIP AUTOMATIC CLIPS MEDIUM 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 K841549.
When did HEMOCLIP AUTOMATIC CLIPS MEDIUM receive FDA 510(k) clearance?
HEMOCLIP AUTOMATIC CLIPS MEDIUM received FDA 510(k) clearance on 1984-08-14, under 510(k) number K841549.
Who is the listed applicant for HEMOCLIP AUTOMATIC CLIPS MEDIUM?
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 AUTOMATIC CLIPS MEDIUM?
The FDA product code for HEMOCLIP AUTOMATIC CLIPS MEDIUM 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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