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FDA 510(k)

BURR, CORNEAL, BATTERY-POWERED

K-Number: K950520 · 1995-05-02

ApplicantAaron Medical Industries
Decision Date1995-05-02
Product CodeHOG
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

BURR, CORNEAL, BATTERY-POWERED is the device name listed in this FDA 510(k) record. The listed applicant is Aaron Medical Industries. It received FDA 510(k) clearance on 1995-05-02 under 510(k) number K950520. 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 BURR, CORNEAL, BATTERY-POWERED?

BURR, CORNEAL, BATTERY-POWERED is a medical device that received FDA 510(k) clearance on 1995-05-02. The listed applicant is Aaron Medical Industries. The 510(k) number is K950520.

When did BURR, CORNEAL, BATTERY-POWERED receive FDA 510(k) clearance?

BURR, CORNEAL, BATTERY-POWERED received FDA 510(k) clearance on 1995-05-02, under 510(k) number K950520.

Who is the listed applicant for BURR, CORNEAL, BATTERY-POWERED?

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

What is the FDA product code for BURR, CORNEAL, BATTERY-POWERED?

The FDA product code for BURR, CORNEAL, BATTERY-POWERED is HOG.

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Other records listing Aaron Medical Industries as applicant

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K062337MODULAR LAPAROSCOPY ACCESSORIES, HANDLE; SISSORS (STRAIGHT AND CURVED); GRASPER (AGGRESSIVE, ALLIS, ATAUMATIC; DISSECTORK061307BOVIE INAFLASH SUTURE REMOVER HANDLE,CHARGER,HANDLE AND CHARGER,KIT,BATTERY PACKK060117BOVIE BUTTON REMOTE HAND SWITCHK022856BOVIE IDS-300 HIGH FREQUENCY ELECTROSURGICAL GENERATORK021817AARON A950 HIGH FREQUENCY ELECTROSURGICAL GENERATOR, AARON A950 ELECTROSURGICAL GENERATOR, 240VK020579AARON ARTHROSCOPY ELECTRODE, CATALOG NUMBERS AR00, AR01, AR02, AND AR03

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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.

K962989AMOILS EPITHELIAL SCRUBBERS. Percy AmoilsK960261PALLIKARIS BRUSHAlcon Laboratories, Inc.K883785GY-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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