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FDA 510(k)

SILVERAK

K-Number: K833838 · 1984-03-02

ApplicantAnil S. Gautam
Decision Date1984-03-02
Product CodeLCN
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SILVERAK is the device name listed in this FDA 510(k) record. The listed applicant is Anil S. Gautam. It received FDA 510(k) clearance on 1984-03-02 under 510(k) number K833838. The device is classified under product code LCN. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SILVERAK?

SILVERAK is a medical device that received FDA 510(k) clearance on 1984-03-02. The listed applicant is Anil S. Gautam. The 510(k) number is K833838.

When did SILVERAK receive FDA 510(k) clearance?

SILVERAK received FDA 510(k) clearance on 1984-03-02, under 510(k) number K833838.

Who is the listed applicant for SILVERAK?

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

What is the FDA product code for SILVERAK?

The FDA product code for SILVERAK is LCN.

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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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