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FDA 510(k)

GORSK INSTRUMENT REST

K-Number: K873554 · 1987-10-23

ApplicantGorsk, Inc.
Decision Date1987-10-23
Product CodeHMG
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

GORSK INSTRUMENT REST is the device name listed in this FDA 510(k) record. The listed applicant is Gorsk, Inc.. It received FDA 510(k) clearance on 1987-10-23 under 510(k) number K873554. The device is classified under product code HMG. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GORSK INSTRUMENT REST?

GORSK INSTRUMENT REST is a medical device that received FDA 510(k) clearance on 1987-10-23. The listed applicant is Gorsk, Inc.. The 510(k) number is K873554.

When did GORSK INSTRUMENT REST receive FDA 510(k) clearance?

GORSK INSTRUMENT REST received FDA 510(k) clearance on 1987-10-23, under 510(k) number K873554.

Who is the listed applicant for GORSK INSTRUMENT REST?

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

What is the FDA product code for GORSK INSTRUMENT REST?

The FDA product code for GORSK INSTRUMENT REST is HMG.

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 Gorsk, 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.

K873555GORSK SPONGE CONTAINMENT SYSTEM

Related Devices (Code: HMG)

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.

K900161A-SCAN ROLL-AROUND STANDJedmed Instrument Co.K883575MODIFIED SITE MOBILE STAND FOR OPHTHALMIC USESite Microsurgical Systems, Inc.K841759OPHTHALMIC TABLEWoodlyn, Inc.

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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