DRY & STORE
K-Number: K972776 · 1997-09-08
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Device Summary
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
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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