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FDA 510(k)

PLASTER TABLE 1418

K-Number: K873274 · 1987-09-17

ApplicantStierlen-Maquet AG
Decision Date1987-09-17
Product CodeJEB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PLASTER TABLE 1418 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 1987-09-17 under 510(k) number K873274. The device is classified under product code JEB. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PLASTER TABLE 1418?

PLASTER TABLE 1418 is a medical device that received FDA 510(k) clearance on 1987-09-17. The listed applicant is Stierlen-Maquet AG. The 510(k) number is K873274.

When did PLASTER TABLE 1418 receive FDA 510(k) clearance?

PLASTER TABLE 1418 received FDA 510(k) clearance on 1987-09-17, under 510(k) number K873274.

Who is the listed applicant for PLASTER TABLE 1418?

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 PLASTER TABLE 1418?

The FDA product code for PLASTER TABLE 1418 is JEB.

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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 1140K883613OPER. TABLE FOR PERCUTAN. TRANS. CORONARY ANGIO.K873275EXTENSION TABLE 1417K873273ORTHOPAEDIC TABLE 1420

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Related Devices (Code: JEB)

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.

K905816ORTHOVISION TABLEAmerican Sterilizer Co.K900405SCHOLTEN FRAMEScholten Surgical Instruments, Inc.K891917ORTHO-J, INC. BEK-JS-004Ortho-J, Inc.K891387WILLIAMS BELT & BOOTArthro-Medic, Inc.K881101K ORTHOPEDIC TABLEInstrumentation Specialties, Inc.K880263OSI RIZZOLI ORTHOPEDIC TABLE/MANUAL VERSIONOrthopedic Systems, 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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