Easytop

FDA 510(k) K853281 · Hydro-Med Products, Inc.

Substantially Equivalent

510(k) numberK853281

Submission

Device name
Easytop
Applicant
Hydro-Med Products, Inc.
Dallas, TX, US
Received
August 5, 1985
Decision date
August 21, 1985
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

No product code recorded.

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Questions and answers

When was Easytop cleared by the FDA?

Easytop (K853281) received a 510(k) decision of Substantially Equivalent on August 21, 1985, 16 days after the submission was received.