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FDA 510(k)

AMOILS EPITHELIAL SCRUBBER

K-Number: K962989 · 1997-01-09

ApplicantS. Percy Amoils
Decision Date1997-01-09
Product CodeHOG
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

AMOILS EPITHELIAL SCRUBBER is the device name listed in this FDA 510(k) record. The listed applicant is S. Percy Amoils. It received FDA 510(k) clearance on 1997-01-09 under 510(k) number K962989. 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 AMOILS EPITHELIAL SCRUBBER?

AMOILS EPITHELIAL SCRUBBER is a medical device that received FDA 510(k) clearance on 1997-01-09. The listed applicant is S. Percy Amoils. The 510(k) number is K962989.

When did AMOILS EPITHELIAL SCRUBBER receive FDA 510(k) clearance?

AMOILS EPITHELIAL SCRUBBER received FDA 510(k) clearance on 1997-01-09, under 510(k) number K962989.

Who is the listed applicant for AMOILS EPITHELIAL SCRUBBER?

The FDA 510(k) record lists S. Percy Amoils as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AMOILS EPITHELIAL SCRUBBER?

The FDA product code for AMOILS EPITHELIAL SCRUBBER is HOG.

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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.

K960261PALLIKARIS BRUSHAlcon Laboratories, Inc.K950520BURR, CORNEAL, BATTERY-POWEREDAaron Medical IndustriesK883785GY-RO SAFEGy-Ro Industry, Inc.K834354OPHTEC 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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