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FDA 510(k)

FAST VIOLET B

K-Number: K821038 · 1982-05-27

ApplicantDms Laboratories
Decision Date1982-05-27
Product CodeJTS
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

FAST VIOLET B is the device name listed in this FDA 510(k) record. The listed applicant is Dms Laboratories. It received FDA 510(k) clearance on 1982-05-27 under 510(k) number K821038. The device is classified under product code JTS. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FAST VIOLET B?

FAST VIOLET B is a medical device that received FDA 510(k) clearance on 1982-05-27. The listed applicant is Dms Laboratories. The 510(k) number is K821038.

When did FAST VIOLET B receive FDA 510(k) clearance?

FAST VIOLET B received FDA 510(k) clearance on 1982-05-27, under 510(k) number K821038.

Who is the listed applicant for FAST VIOLET B?

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 FAST VIOLET B?

The FDA product code for FAST VIOLET B is JTS.

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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.

K831186RAPID NFTK831187TRPK830437CHSK823102AGAR PK813613RAPID CHK813612RAPID ZYME

View all 23 devices →

Related Devices (Code: JTS)

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.

K960095BACTIDROP CALCOFLUOR WHITERemel Co.K960090CALCOFLUOR WHITE STAIN KITRemel Co.K920970BACTIDROP KOH (10%)Remel Co.K920975BACTIDROP CALCOFLUOR WHITERemel Co.K920976BACTIDROP INDIA INKRemel Co.K893530IRISTAIN FORMULA 2, PARTS 1 AND 2Intl. Remote Imaging Systems

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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