Mobile Operating Table for Orl Microsurgery

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K853720 ↗

FDA Product Code

GDC

Device Class

Class I

Regulation

21 CFR Part 878.4960

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

• S 21 Instrument Stand

  Class I

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  Class II

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• S 22 Instrument Stand

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  Class II

  FDA 510(k) K983868 Active Cleared 29 Jan 1999

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See all devices from Carl Zeiss, Inc. →