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FDA 510(k)

VARIOUS SURG. & DIAGNOSTIC INSTRU. ETC.

K-Number: K770428 · 1979-09-12

Decision Date1979-09-12
Product CodeFSM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VARIOUS SURG. & DIAGNOSTIC INSTRU. ETC. is the device name listed in this FDA 510(k) record. The listed applicant is Holco Instrument Corp.. It received FDA 510(k) clearance on 1979-09-12 under 510(k) number K770428. The device is classified under product code FSM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VARIOUS SURG. & DIAGNOSTIC INSTRU. ETC.?

VARIOUS SURG. & DIAGNOSTIC INSTRU. ETC. is a medical device that received FDA 510(k) clearance on 1979-09-12. The listed applicant is Holco Instrument Corp.. The 510(k) number is K770428.

When did VARIOUS SURG. & DIAGNOSTIC INSTRU. ETC. receive FDA 510(k) clearance?

VARIOUS SURG. & DIAGNOSTIC INSTRU. ETC. received FDA 510(k) clearance on 1979-09-12, under 510(k) number K770428.

Who is the listed applicant for VARIOUS SURG. & DIAGNOSTIC INSTRU. ETC.?

The FDA 510(k) record lists Holco Instrument Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VARIOUS SURG. & DIAGNOSTIC INSTRU. ETC.?

The FDA product code for VARIOUS SURG. & DIAGNOSTIC INSTRU. ETC. is FSM.

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 Holco Instrument 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: FSM)

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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