FDA 510(k)

VP I

K-Number: K820204 · 1982-02-05

Decision Date1982-02-05

Product CodeJTO

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

VP I is the device name listed in this FDA 510(k) record. The listed applicant is Dms Laboratories. It received FDA 510(k) clearance on 1982-02-05 under 510(k) number K820204. The device is classified under product code JTO. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VP I?

VP I is a medical device that received FDA 510(k) clearance on 1982-02-05. The listed applicant is Dms Laboratories. The 510(k) number is K820204.

When did VP I receive FDA 510(k) clearance?

VP I received FDA 510(k) clearance on 1982-02-05, under 510(k) number K820204.

Who is the listed applicant for VP I?

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

What is the FDA product code for VP I?

The FDA product code for VP I is JTO.

Other records listing Dms Laboratories 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.

K831187TRP K831186RAPID NFT K830437CHS K823102AGAR P K821038FAST VIOLET B K813613RAPID CH

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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.