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FDA 510(k)

SURGICAL STAPLE REMOVER

K-Number: K811120 · 1981-05-05

Decision Date1981-05-05
Product CodeKDC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SURGICAL STAPLE REMOVER is the device name listed in this FDA 510(k) record. The listed applicant is Acme United Corp.. It received FDA 510(k) clearance on 1981-05-05 under 510(k) number K811120. The device is classified under product code KDC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGICAL STAPLE REMOVER?

SURGICAL STAPLE REMOVER is a medical device that received FDA 510(k) clearance on 1981-05-05. The listed applicant is Acme United Corp.. The 510(k) number is K811120.

When did SURGICAL STAPLE REMOVER receive FDA 510(k) clearance?

SURGICAL STAPLE REMOVER received FDA 510(k) clearance on 1981-05-05, under 510(k) number K811120.

Who is the listed applicant for SURGICAL STAPLE REMOVER?

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 SURGICAL STAPLE REMOVER?

The FDA product code for SURGICAL STAPLE REMOVER is KDC.

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.

View all 27 devices →

Related Devices (Code: KDC)

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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