EXTENSION DEVICE 1416— 510(k) K873276

Substantially Equivalent

Stierlen-Maquet AG

FDA 510(k) clearance K873276 for EXTENSION DEVICE 1416, Substantially Equivalent on 1987-09-17. Applicant: Stierlen-Maquet AG. Device class: 1.

Clearance details

Applicant: Stierlen-Maquet AG
Product code: Code JEB
Device class: Class 1
Regulation: 21 CFR 878.4950
Advisory panel: General, Plastic Surgery
Date received: 1987-08-17
Decision date: 1987-09-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: West Germany, GR

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Recent devices under product code JEB

K905816 — ORTHOVISION TABLE1991-03-06
K900405 — SCHOLTEN FRAME1990-03-01
K891917 — ORTHO-J, INC. BEK-JS-0041989-05-26
K891387 — WILLIAMS BELT & BOOT1989-05-23
K881101 — K ORTHOPEDIC TABLE1988-04-06

More clearances from Stierlen-Maquet AG

K970807 — MOBILE OPERATING TABLE 1132.011997-03-14
K926525 — BETASTAR 1131.02 MOBILE OPERATING TABLE1993-10-12
K920890 — OPERATING TABLE SYSTEM-BETAMAQUET 11401992-07-02
K883613 — OPER. TABLE FOR PERCUTAN. TRANS. CORONARY ANGIO.1988-09-15
K873273 — ORTHOPAEDIC TABLE 14201987-09-17

Data sourced from openFDA. This site is unofficial and independent of the FDA.