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FDA 510(k)

MODIFICATION OF ANTERIOR SEGMENT ELECTRODES

K-Number: K933527 · 1994-01-25

ApplicantMira, Inc.
Decision Date1994-01-25
Product CodeHWA
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MODIFICATION OF ANTERIOR SEGMENT ELECTRODES is the device name listed in this FDA 510(k) record. The listed applicant is Mira, Inc.. It received FDA 510(k) clearance on 1994-01-25 under 510(k) number K933527. The device is classified under product code HWA. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFICATION OF ANTERIOR SEGMENT ELECTRODES?

MODIFICATION OF ANTERIOR SEGMENT ELECTRODES is a medical device that received FDA 510(k) clearance on 1994-01-25. The listed applicant is Mira, Inc.. The 510(k) number is K933527.

When did MODIFICATION OF ANTERIOR SEGMENT ELECTRODES receive FDA 510(k) clearance?

MODIFICATION OF ANTERIOR SEGMENT ELECTRODES received FDA 510(k) clearance on 1994-01-25, under 510(k) number K933527.

Who is the listed applicant for MODIFICATION OF ANTERIOR SEGMENT ELECTRODES?

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

What is the FDA product code for MODIFICATION OF ANTERIOR SEGMENT ELECTRODES?

The FDA product code for MODIFICATION OF ANTERIOR SEGMENT ELECTRODES is HWA.

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Other records listing Mira, 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.

K951728SCHEPENS-YOSHIDA VIDEO BINOCULAR INDIRECT OPHTHALMSCOPEK950806SOLID DILICONE IMPLANTS, SDILICONE SPONGE IMPLANTSK941495RETURN PATH DIATHERMY HANDLEK923629OPHTHALMIC TRICHIASIS PROBEK894248CONVERTER SYSTEMK891601POWER OPERATED AND CONTROLLED VITREOUS SCISSORS

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Related Devices (Code: HWA)

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.

K864422RAYLOR(TM) MALLETCedar Surgical, Inc.K841627MALLETPlastafil, Inc.K770205CEMENT CHISELSDepuy, 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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