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FDA 510(k)

MOBILE OPERATING TABLE 1132.01

K-Number: K970807 · 1997-03-14

ApplicantStierlen-Maquet AG
Decision Date1997-03-14
Product CodeGDC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MOBILE OPERATING TABLE 1132.01 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 1997-03-14 under 510(k) number K970807. The device is classified under product code GDC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOBILE OPERATING TABLE 1132.01?

MOBILE OPERATING TABLE 1132.01 is a medical device that received FDA 510(k) clearance on 1997-03-14. The listed applicant is Stierlen-Maquet AG. The 510(k) number is K970807.

When did MOBILE OPERATING TABLE 1132.01 receive FDA 510(k) clearance?

MOBILE OPERATING TABLE 1132.01 received FDA 510(k) clearance on 1997-03-14, under 510(k) number K970807.

Who is the listed applicant for MOBILE OPERATING TABLE 1132.01?

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 MOBILE OPERATING TABLE 1132.01?

The FDA product code for MOBILE OPERATING TABLE 1132.01 is GDC.

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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.

K926525BETASTAR 1131.02 MOBILE OPERATING TABLEK920890OPERATING TABLE SYSTEM-BETAMAQUET 1140K883613OPER. TABLE FOR PERCUTAN. TRANS. CORONARY ANGIO.K873276EXTENSION DEVICE 1416K873275EXTENSION TABLE 1417K873273ORTHOPAEDIC TABLE 1420

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Related Devices (Code: GDC)

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.

K971390QUANTUM 3080SP SURGICAL TABLESTERIS CorporationK964273DURA-BOARD ARMBOARDAllen Medical Systems, Inc.K940616SKYTRON ELITE 3500 TABLESkytron, Div. the Kmw Group, Inc.K934744MIDMARK MAGNUM GENERAL SURGICAL TABLEMidmark Corp.K914758MDT/SHAMPAINE MODEL 4900B SURGICAL TABLEMdt Corp., Inc.K915393MDT/SHAMPAINE MODEL 4900E SURGICAL TABLEMdt Corp., Inc.

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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