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FDA 510(k)

SURGICRAFT COPELAND DISPOSABLE

K-Number: K844608 · 1985-05-01

ApplicantA.W. Showell (Surgicraft) , Ltd.
Decision Date1985-05-01
Product CodeHGP
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SURGICRAFT COPELAND DISPOSABLE is the device name listed in this FDA 510(k) record. The listed applicant is A.W. Showell (Surgicraft) , Ltd.. It received FDA 510(k) clearance on 1985-05-01 under 510(k) number K844608. The device is classified under product code HGP. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGICRAFT COPELAND DISPOSABLE?

SURGICRAFT COPELAND DISPOSABLE is a medical device that received FDA 510(k) clearance on 1985-05-01. The listed applicant is A.W. Showell (Surgicraft) , Ltd.. The 510(k) number is K844608.

When did SURGICRAFT COPELAND DISPOSABLE receive FDA 510(k) clearance?

SURGICRAFT COPELAND DISPOSABLE received FDA 510(k) clearance on 1985-05-01, under 510(k) number K844608.

Who is the listed applicant for SURGICRAFT COPELAND DISPOSABLE?

The FDA 510(k) record lists A.W. Showell (Surgicraft) , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SURGICRAFT COPELAND DISPOSABLE?

The FDA product code for SURGICRAFT COPELAND DISPOSABLE is HGP.

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.

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Other records listing A.W. Showell (Surgicraft) , Ltd. 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.

K853033HARTSHILL RECT & WIRES, SPINAL FIXATION SYSTEM

Related Devices (Code: HGP)

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.

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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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