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FDA 510(k)

INTRAOCULAR ELECTROMAGNET

K-Number: K854870 · 1986-02-19

ApplicantMira, Inc.
Decision Date1986-02-19
Product CodeHPO
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

INTRAOCULAR ELECTROMAGNET is the device name listed in this FDA 510(k) record. The listed applicant is Mira, Inc.. It received FDA 510(k) clearance on 1986-02-19 under 510(k) number K854870. The device is classified under product code HPO. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTRAOCULAR ELECTROMAGNET?

INTRAOCULAR ELECTROMAGNET is a medical device that received FDA 510(k) clearance on 1986-02-19. The listed applicant is Mira, Inc.. The 510(k) number is K854870.

When did INTRAOCULAR ELECTROMAGNET receive FDA 510(k) clearance?

INTRAOCULAR ELECTROMAGNET received FDA 510(k) clearance on 1986-02-19, under 510(k) number K854870.

Who is the listed applicant for INTRAOCULAR ELECTROMAGNET?

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 INTRAOCULAR ELECTROMAGNET?

The FDA product code for INTRAOCULAR ELECTROMAGNET is HPO.

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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 HANDLEK933527MODIFICATION OF ANTERIOR SEGMENT ELECTRODESK923629OPHTHALMIC TRICHIASIS PROBEK894248CONVERTER SYSTEM

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Related Devices (Code: HPO)

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.

K832950SCIENTRONICS 10K EYE MAGNETScientific ManufacturerK830336DORC INTRAOCULAR ELECTROMAGNETJedmed 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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