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FDA 510(k)

MTB 1043 TREATMENT BOOTH

K-Number: K944133 · 1995-09-07

Decision Date1995-09-07
Product CodeLGM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MTB 1043 TREATMENT BOOTH is the device name listed in this FDA 510(k) record. The listed applicant is Mark Solutions, Inc.. It received FDA 510(k) clearance on 1995-09-07 under 510(k) number K944133. The device is classified under product code LGM. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MTB 1043 TREATMENT BOOTH?

MTB 1043 TREATMENT BOOTH is a medical device that received FDA 510(k) clearance on 1995-09-07. The listed applicant is Mark Solutions, Inc.. The 510(k) number is K944133.

When did MTB 1043 TREATMENT BOOTH receive FDA 510(k) clearance?

MTB 1043 TREATMENT BOOTH received FDA 510(k) clearance on 1995-09-07, under 510(k) number K944133.

Who is the listed applicant for MTB 1043 TREATMENT BOOTH?

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

What is the FDA product code for MTB 1043 TREATMENT BOOTH?

The FDA product code for MTB 1043 TREATMENT BOOTH is LGM.

Related Clinical Trials

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.

Related Devices (Code: LGM)

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.

Official Source

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