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FDA 510(k)

EASYTOP

K-Number: K853281 · 1985-08-21

Decision Date1985-08-21
Product Code
DecisionSubstantially Equivalent

Device Summary

EASYTOP is the device name listed in this FDA 510(k) record. The listed applicant is Hydro-Med Products, Inc.. It received FDA 510(k) clearance on 1985-08-21 under 510(k) number K853281. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EASYTOP?

EASYTOP is a medical device that received FDA 510(k) clearance on 1985-08-21. The listed applicant is Hydro-Med Products, Inc.. The 510(k) number is K853281.

When did EASYTOP receive FDA 510(k) clearance?

EASYTOP received FDA 510(k) clearance on 1985-08-21, under 510(k) number K853281.

Who is the listed applicant for EASYTOP?

The FDA 510(k) record lists Hydro-Med Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

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 Hydro-Med Products, 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.

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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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