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FDA 510(k)

PERFECT EAR/PE

K-Number: K931984 · 1993-06-08

ApplicantPerfect Ear
Decision Date1993-06-08
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

PERFECT EAR/PE is the device name listed in this FDA 510(k) record. The listed applicant is Perfect Ear. It received FDA 510(k) clearance on 1993-06-08 under 510(k) number K931984. The device is classified under product code ESD. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERFECT EAR/PE?

PERFECT EAR/PE is a medical device that received FDA 510(k) clearance on 1993-06-08. The listed applicant is Perfect Ear. The 510(k) number is K931984.

When did PERFECT EAR/PE receive FDA 510(k) clearance?

PERFECT EAR/PE received FDA 510(k) clearance on 1993-06-08, under 510(k) number K931984.

Who is the listed applicant for PERFECT EAR/PE?

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

What is the FDA product code for PERFECT EAR/PE?

The FDA product code for PERFECT EAR/PE is ESD.

Related Clinical Trials

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.

Other records listing Perfect Ear 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.

Related Devices (Code: ESD)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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