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FDA 510(k)

SURGICAL INSTRUMENT PROTECTOR

K-Number: K771123 · 1977-10-28

Decision Date1977-10-28
Product CodeKCT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SURGICAL INSTRUMENT PROTECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Devon Industries, Inc.. It received FDA 510(k) clearance on 1977-10-28 under 510(k) number K771123. The device is classified under product code KCT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGICAL INSTRUMENT PROTECTOR?

SURGICAL INSTRUMENT PROTECTOR is a medical device that received FDA 510(k) clearance on 1977-10-28. The listed applicant is Devon Industries, Inc.. The 510(k) number is K771123.

When did SURGICAL INSTRUMENT PROTECTOR receive FDA 510(k) clearance?

SURGICAL INSTRUMENT PROTECTOR received FDA 510(k) clearance on 1977-10-28, under 510(k) number K771123.

Who is the listed applicant for SURGICAL INSTRUMENT PROTECTOR?

The FDA 510(k) record lists Devon Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SURGICAL INSTRUMENT PROTECTOR?

The FDA product code for SURGICAL INSTRUMENT PROTECTOR is KCT.

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 Devon Industries, 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.

View all 47 devices →

Related Devices (Code: KCT)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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