APPOSE SKIN STAPLER
K-Number: K811030 · 1981-05-27
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Device Summary
Frequently Asked Questions
What is the APPOSE SKIN STAPLER?
APPOSE SKIN STAPLER is a medical device that received FDA 510(k) clearance on 1981-05-27. The listed applicant is Davis & Geck, Inc.. The 510(k) number is K811030.
When did APPOSE SKIN STAPLER receive FDA 510(k) clearance?
APPOSE SKIN STAPLER received FDA 510(k) clearance on 1981-05-27, under 510(k) number K811030.
Who is the listed applicant for APPOSE SKIN STAPLER?
The FDA 510(k) record lists Davis & Geck, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for APPOSE SKIN STAPLER?
The FDA product code for APPOSE SKIN STAPLER is GAG.
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 Davis & Geck, 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: GAG)
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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