Wee Bag O'mercury

No FDA recalls on record, checked 10 Oct 2026.

510(k) Number

K840004 ↗

FDA Product Code

LCC

Device Class

Class II

Regulation

21 CFR Part 886.4610

Advisory Committee

Ophthalmic

FDA Decision

SESE Substantially Equivalent

• Charles/Mcintyre Giant Break Table

  Class I

  FDA 510(k) K841115 Active Cleared 9 May 1984

• Surgi-Quip Microscope Stand

  Class I

  FDA 510(k) K822428 Active Cleared 2 Sep 1982

• Cement Extraction Instrumentation

  Not classified

  FDA 510(k) K822554 Active Cleared 14 Sep 1982

• Mobile Ophthalmic Operating Table

  Class I

  FDA 510(k) K841116 Active Cleared 9 May 1984

• Electronic Unit

  Class I

  FDA 510(k) K832887 Active Cleared 4 Oct 1983

• Self-Contained Mobile Ophthal. Oper. .

  Class I

  FDA 510(k) K822427 Active Cleared 14 Sep 1982

See all devices from Surgi-Quip Inc.U →