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FDA 510(k)

GY-RO SAFE

K-Number: K883785 · 1989-01-05

ApplicantGy-Ro Industry, Inc.
Decision Date1989-01-05
Product CodeHOG
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

GY-RO SAFE is the device name listed in this FDA 510(k) record. The listed applicant is Gy-Ro Industry, Inc.. It received FDA 510(k) clearance on 1989-01-05 under 510(k) number K883785. The device is classified under product code HOG. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GY-RO SAFE?

GY-RO SAFE is a medical device that received FDA 510(k) clearance on 1989-01-05. The listed applicant is Gy-Ro Industry, Inc.. The 510(k) number is K883785.

When did GY-RO SAFE receive FDA 510(k) clearance?

GY-RO SAFE received FDA 510(k) clearance on 1989-01-05, under 510(k) number K883785.

Who is the listed applicant for GY-RO SAFE?

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

What is the FDA product code for GY-RO SAFE?

The FDA product code for GY-RO SAFE is HOG.

Related Devices (Code: HOG)

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.

K962989AMOILS EPITHELIAL SCRUBBERS. Percy AmoilsK960261PALLIKARIS BRUSHAlcon Laboratories, Inc.K950520BURR, CORNEAL, BATTERY-POWEREDAaron Medical IndustriesK834354OPHTEC RUST RING REMOVERJedmed Instrument Co.

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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