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FDA 510(k)

CORRECT-A-COUNT

K-Number: K853374 · 1985-09-05

Decision Date1985-09-05
Product Code
DecisionSubstantially Equivalent

Device Summary

CORRECT-A-COUNT is the device name listed in this FDA 510(k) record. The listed applicant is Dermacare Products, Inc.. It received FDA 510(k) clearance on 1985-09-05 under 510(k) number K853374. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CORRECT-A-COUNT?

CORRECT-A-COUNT is a medical device that received FDA 510(k) clearance on 1985-09-05. The listed applicant is Dermacare Products, Inc.. The 510(k) number is K853374.

When did CORRECT-A-COUNT receive FDA 510(k) clearance?

CORRECT-A-COUNT received FDA 510(k) clearance on 1985-09-05, under 510(k) number K853374.

Who is the listed applicant for CORRECT-A-COUNT?

The FDA 510(k) record lists Dermacare 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 Dermacare 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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