REPROCESSED MULTIPLE CLIP APPLIERS
K-Number: K033579 · 2005-07-11
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Device Summary
Frequently Asked Questions
What is the REPROCESSED MULTIPLE CLIP APPLIERS?
REPROCESSED MULTIPLE CLIP APPLIERS is a medical device that received FDA 510(k) clearance on 2005-07-11. The listed applicant is Clearmedical, Inc.. The 510(k) number is K033579.
When did REPROCESSED MULTIPLE CLIP APPLIERS receive FDA 510(k) clearance?
REPROCESSED MULTIPLE CLIP APPLIERS received FDA 510(k) clearance on 2005-07-11, under 510(k) number K033579.
Who is the listed applicant for REPROCESSED MULTIPLE CLIP APPLIERS?
The FDA 510(k) record lists Clearmedical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for REPROCESSED MULTIPLE CLIP APPLIERS?
The FDA product code for REPROCESSED MULTIPLE CLIP APPLIERS is NMJ.
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 Clearmedical, 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.
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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