APPOSE ULE STERILE DISPOS. SKIN STAP
K-Number: K840177 · 1984-03-05
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Device Summary
Frequently Asked Questions
What is the APPOSE ULE STERILE DISPOS. SKIN STAP?
APPOSE ULE STERILE DISPOS. SKIN STAP is a medical device that received FDA 510(k) clearance on 1984-03-05. The listed applicant is Davis & Geck, Inc.. The 510(k) number is K840177.
When did APPOSE ULE STERILE DISPOS. SKIN STAP receive FDA 510(k) clearance?
APPOSE ULE STERILE DISPOS. SKIN STAP received FDA 510(k) clearance on 1984-03-05, under 510(k) number K840177.
Who is the listed applicant for APPOSE ULE STERILE DISPOS. SKIN STAP?
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 ULE STERILE DISPOS. SKIN STAP?
The FDA product code for APPOSE ULE STERILE DISPOS. SKIN STAP 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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