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FDA 510(k)

DERMASCAN C, AN ULTRASONIC DIAGNOSTIC SYSTEM

K-Number: K894834 · 1989-10-02

ApplicantBrymill Corp.
Decision Date1989-10-02
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DERMASCAN C, AN ULTRASONIC DIAGNOSTIC SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Brymill Corp.. It received FDA 510(k) clearance on 1989-10-02 under 510(k) number K894834. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DERMASCAN C, AN ULTRASONIC DIAGNOSTIC SYSTEM?

DERMASCAN C, AN ULTRASONIC DIAGNOSTIC SYSTEM is a medical device that received FDA 510(k) clearance on 1989-10-02. The listed applicant is Brymill Corp.. The 510(k) number is K894834.

When did DERMASCAN C, AN ULTRASONIC DIAGNOSTIC SYSTEM receive FDA 510(k) clearance?

DERMASCAN C, AN ULTRASONIC DIAGNOSTIC SYSTEM received FDA 510(k) clearance on 1989-10-02, under 510(k) number K894834.

Who is the listed applicant for DERMASCAN C, AN ULTRASONIC DIAGNOSTIC SYSTEM?

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

What is the FDA product code for DERMASCAN C, AN ULTRASONIC DIAGNOSTIC SYSTEM?

The FDA product code for DERMASCAN C, AN ULTRASONIC DIAGNOSTIC SYSTEM is IYO.

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Other records listing Brymill 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.

K072453CRY-AC TRACKER, MODEL(S) B-700T, AND B-800TK881336BRYMASCAN-A

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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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