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FDA 510(k)

PHONIC MIRROR HANDIVOCIE MODEL 110

K-Number: K772346 · 1978-01-11

ApplicantHc Electronics
Decision Date1978-01-11
Product Code
DecisionSubstantially Equivalent

Device Summary

PHONIC MIRROR HANDIVOCIE MODEL 110 is the device name listed in this FDA 510(k) record. The listed applicant is Hc Electronics. It received FDA 510(k) clearance on 1978-01-11 under 510(k) number K772346. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHONIC MIRROR HANDIVOCIE MODEL 110?

PHONIC MIRROR HANDIVOCIE MODEL 110 is a medical device that received FDA 510(k) clearance on 1978-01-11. The listed applicant is Hc Electronics. The 510(k) number is K772346.

When did PHONIC MIRROR HANDIVOCIE MODEL 110 receive FDA 510(k) clearance?

PHONIC MIRROR HANDIVOCIE MODEL 110 received FDA 510(k) clearance on 1978-01-11, under 510(k) number K772346.

Who is the listed applicant for PHONIC MIRROR HANDIVOCIE MODEL 110?

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

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Other records listing Hc Electronics 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.

K810031STEREO AUDITORY TRAINER (MODEL PM228)K810030POST-AURICULAR HEARING AID (#PE830)K800340PHONIC EAR, MODEL 841LK782053HEARING AID, POST-AURICULARK780936PHONIC EARK780363PHONIC EAR

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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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