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FDA 510(k)

OPHTHALMIC CAUTERY

K-Number: K945493 · 1995-01-30

ApplicantAaron Medical Industries
Decision Date1995-01-30
Product CodeHQP
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

OPHTHALMIC CAUTERY 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 1995-01-30 under 510(k) number K945493. The device is classified under product code HQP. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OPHTHALMIC CAUTERY?

OPHTHALMIC CAUTERY is a medical device that received FDA 510(k) clearance on 1995-01-30. The listed applicant is Aaron Medical Industries. The 510(k) number is K945493.

When did OPHTHALMIC CAUTERY receive FDA 510(k) clearance?

OPHTHALMIC CAUTERY received FDA 510(k) clearance on 1995-01-30, under 510(k) number K945493.

Who is the listed applicant for OPHTHALMIC CAUTERY?

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 OPHTHALMIC CAUTERY?

The FDA product code for OPHTHALMIC CAUTERY is HQP.

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Other records listing Aaron Medical Industries 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.

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

View all 46 devices →

Related Devices (Code: HQP)

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.

K121441CAUTERY; LOW TEMPERATURE (FINEADJUSTABLE FINE TIP, ELONGATED FINE TIP, MICRO FINE TIP)Bovie Medical CorporationK083428F7244, F7255, F7266, F7277, F7288, F7233, F7234 SERIES OF BATTERY-POWERED CAUTERYFiab SpaK062659KIRWAN DISPOSABLE BATTERY-POWERED CAUTERY, MODEL 41-61XX SERIESKirwan Surgical Products, Inc.K023506SURGICAL MEDICAL DEVICE CAUTERYModern Medical Equipment Mfg., Ltd.K002547STARION INSTRUMENTS POWER POINT CAUTERY GRASPER/DISSECTORStarion InstrumentsK994019CAUTERY GRASPER/DISSECTORStarion Instruments

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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