APPOSE ULTRA DISPOS. SKIN STAPLER W/AUTO RELEASE
K-Number: K844417 · 1984-12-17
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Device Summary
Frequently Asked Questions
What is the APPOSE ULTRA DISPOS. SKIN STAPLER W/AUTO RELEASE?
APPOSE ULTRA DISPOS. SKIN STAPLER W/AUTO RELEASE is a medical device that received FDA 510(k) clearance on 1984-12-17. The listed applicant is Davis & Geck, Inc.. The 510(k) number is K844417.
When did APPOSE ULTRA DISPOS. SKIN STAPLER W/AUTO RELEASE receive FDA 510(k) clearance?
APPOSE ULTRA DISPOS. SKIN STAPLER W/AUTO RELEASE received FDA 510(k) clearance on 1984-12-17, under 510(k) number K844417.
Who is the listed applicant for APPOSE ULTRA DISPOS. SKIN STAPLER W/AUTO RELEASE?
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 ULTRA DISPOS. SKIN STAPLER W/AUTO RELEASE?
The FDA product code for APPOSE ULTRA DISPOS. SKIN STAPLER W/AUTO RELEASE 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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