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FDA 510(k)

MDT SHAMPAINE 5100B AND 5100E SURGICAL TABLES

K-Number: K941150 · 1994-06-10

ApplicantMdt Technology For Life
Decision Date1994-06-10
Product CodeFQO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MDT SHAMPAINE 5100B AND 5100E SURGICAL TABLES is the device name listed in this FDA 510(k) record. The listed applicant is Mdt Technology For Life. It received FDA 510(k) clearance on 1994-06-10 under 510(k) number K941150. The device is classified under product code FQO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MDT SHAMPAINE 5100B AND 5100E SURGICAL TABLES?

MDT SHAMPAINE 5100B AND 5100E SURGICAL TABLES is a medical device that received FDA 510(k) clearance on 1994-06-10. The listed applicant is Mdt Technology For Life. The 510(k) number is K941150.

When did MDT SHAMPAINE 5100B AND 5100E SURGICAL TABLES receive FDA 510(k) clearance?

MDT SHAMPAINE 5100B AND 5100E SURGICAL TABLES received FDA 510(k) clearance on 1994-06-10, under 510(k) number K941150.

Who is the listed applicant for MDT SHAMPAINE 5100B AND 5100E SURGICAL TABLES?

The FDA 510(k) record lists Mdt Technology For Life as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MDT SHAMPAINE 5100B AND 5100E SURGICAL TABLES?

The FDA product code for MDT SHAMPAINE 5100B AND 5100E SURGICAL TABLES is FQO.

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Related Devices (Code: FQO)

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.

K240598Maestro System (REF100)Moon SurgicalK221410Maestro PlatformMoon SurgicalK090136STERIS CMAX XLT SURGICAL TABLESTERIS CorporationK972810OPT80 THE TRANSPORTABLE (OPT80)O.P.T. USA, Inc.K971988ALLEN, ULTRA AND SMART SOCKETSAllen Medical Systems, Inc.K971307AMSCO SURGICAL TABLESTERIS Corporation

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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