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FDA 510(k)

BETASTAR 1131.02 MOBILE OPERATING TABLE

K-Number: K926525 · 1993-10-12

ApplicantStierlen-Maquet AG
Decision Date1993-10-12
Product CodeFQO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BETASTAR 1131.02 MOBILE OPERATING TABLE is the device name listed in this FDA 510(k) record. The listed applicant is Stierlen-Maquet AG. It received FDA 510(k) clearance on 1993-10-12 under 510(k) number K926525. 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 BETASTAR 1131.02 MOBILE OPERATING TABLE?

BETASTAR 1131.02 MOBILE OPERATING TABLE is a medical device that received FDA 510(k) clearance on 1993-10-12. The listed applicant is Stierlen-Maquet AG. The 510(k) number is K926525.

When did BETASTAR 1131.02 MOBILE OPERATING TABLE receive FDA 510(k) clearance?

BETASTAR 1131.02 MOBILE OPERATING TABLE received FDA 510(k) clearance on 1993-10-12, under 510(k) number K926525.

Who is the listed applicant for BETASTAR 1131.02 MOBILE OPERATING TABLE?

The FDA 510(k) record lists Stierlen-Maquet AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BETASTAR 1131.02 MOBILE OPERATING TABLE?

The FDA product code for BETASTAR 1131.02 MOBILE OPERATING TABLE is FQO.

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Other records listing Stierlen-Maquet AG 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.

K970807MOBILE OPERATING TABLE 1132.01K920890OPERATING TABLE SYSTEM-BETAMAQUET 1140K883613OPER. TABLE FOR PERCUTAN. TRANS. CORONARY ANGIO.K873276EXTENSION DEVICE 1416K873275EXTENSION TABLE 1417K873273ORTHOPAEDIC TABLE 1420

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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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