ONE TIME DISPOSABLE SKIN STAPLER
K-Number: K830704 · 1983-04-12
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Device Summary
Frequently Asked Questions
What is the ONE TIME DISPOSABLE SKIN STAPLER?
ONE TIME DISPOSABLE SKIN STAPLER is a medical device that received FDA 510(k) clearance on 1983-04-12. The listed applicant is Acme United Corp.. The 510(k) number is K830704.
When did ONE TIME DISPOSABLE SKIN STAPLER receive FDA 510(k) clearance?
ONE TIME DISPOSABLE SKIN STAPLER received FDA 510(k) clearance on 1983-04-12, under 510(k) number K830704.
Who is the listed applicant for ONE TIME DISPOSABLE SKIN STAPLER?
The FDA 510(k) record lists Acme United Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ONE TIME DISPOSABLE SKIN STAPLER?
The FDA product code for ONE TIME DISPOSABLE SKIN STAPLER is FZQ.
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 Acme United Corp. 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: FZQ)
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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