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FDA 510(k)

OPER. TABLE FOR PERCUTAN. TRANS. CORONARY ANGIO.

K-Number: K883613 · 1988-09-15

ApplicantStierlen-Maquet AG
Decision Date1988-09-15
Product CodeGDC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

OPER. TABLE FOR PERCUTAN. TRANS. CORONARY ANGIO. 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 1988-09-15 under 510(k) number K883613. 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 OPER. TABLE FOR PERCUTAN. TRANS. CORONARY ANGIO.?

OPER. TABLE FOR PERCUTAN. TRANS. CORONARY ANGIO. is a medical device that received FDA 510(k) clearance on 1988-09-15. The listed applicant is Stierlen-Maquet AG. The 510(k) number is K883613.

When did OPER. TABLE FOR PERCUTAN. TRANS. CORONARY ANGIO. receive FDA 510(k) clearance?

OPER. TABLE FOR PERCUTAN. TRANS. CORONARY ANGIO. received FDA 510(k) clearance on 1988-09-15, under 510(k) number K883613.

Who is the listed applicant for OPER. TABLE FOR PERCUTAN. TRANS. CORONARY ANGIO.?

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 OPER. TABLE FOR PERCUTAN. TRANS. CORONARY ANGIO.?

The FDA product code for OPER. TABLE FOR PERCUTAN. TRANS. CORONARY ANGIO. 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.

K970807MOBILE OPERATING TABLE 1132.01K926525BETASTAR 1131.02 MOBILE OPERATING TABLEK920890OPERATING TABLE SYSTEM-BETAMAQUET 1140K873276EXTENSION DEVICE 1416K873275EXTENSION TABLE 1417K873273ORTHOPAEDIC TABLE 1420

View all 10 devices →

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 CorporationK970807MOBILE OPERATING TABLE 1132.01Stierlen-Maquet AGK964273DURA-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.

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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