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FDA 510(k)

SILVERSTEIN MICROWICK

K-Number: K991670 · 1999-08-26

ApplicantMicromedics, Inc.
Decision Date1999-08-26
Product CodeETD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

SILVERSTEIN MICROWICK is the device name listed in this FDA 510(k) record. The listed applicant is Micromedics, Inc.. It received FDA 510(k) clearance on 1999-08-26 under 510(k) number K991670. The device is classified under product code ETD. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SILVERSTEIN MICROWICK?

SILVERSTEIN MICROWICK is a medical device that received FDA 510(k) clearance on 1999-08-26. The listed applicant is Micromedics, Inc.. The 510(k) number is K991670.

When did SILVERSTEIN MICROWICK receive FDA 510(k) clearance?

SILVERSTEIN MICROWICK received FDA 510(k) clearance on 1999-08-26, under 510(k) number K991670.

Who is the listed applicant for SILVERSTEIN MICROWICK?

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

What is the FDA product code for SILVERSTEIN MICROWICK?

The FDA product code for SILVERSTEIN MICROWICK is ETD.

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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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