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FDA 510(k)

DRY & STORE

K-Number: K972776 · 1997-09-08

Decision Date1997-09-08
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

DRY & STORE is the device name listed in this FDA 510(k) record. The listed applicant is Ear Technology Corp.. It received FDA 510(k) clearance on 1997-09-08 under 510(k) number K972776. 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 DRY & STORE?

DRY & STORE is a medical device that received FDA 510(k) clearance on 1997-09-08. The listed applicant is Ear Technology Corp.. The 510(k) number is K972776.

When did DRY & STORE receive FDA 510(k) clearance?

DRY & STORE received FDA 510(k) clearance on 1997-09-08, under 510(k) number K972776.

Who is the listed applicant for DRY & STORE?

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

What is the FDA product code for DRY & STORE?

The FDA product code for DRY & STORE 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 Ear Technology Corp. 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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