Skytron Model 1100 and Model 142

No FDA recalls found in the data synced 11 Oct 2026.

510(k) Number

K900290 ↗

FDA Product Code

JEA

Device Class

Class I

Regulation

21 CFR Part 878.4960

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

• Stellar

  Class II

  FDA 510(k) K002463 Active Cleared 8 Nov 2000

• Skytron Elite 300 Surgery Table

  Class I

  FDA 510(k) K853479 Active Cleared 5 Sep 1985

• Skytron Universe Series Surgical Lights

  Class II

  FDA 510(k) K900211 Active Cleared 19 Mar 1990

• Skytron Model 610-2

  Class II

  FDA 510(k) K870045 Active Cleared 4 Feb 1987

• Skytron Model 130 Surgical Table

  Class I

  FDA 510(k) K873478 Active Cleared 24 Sep 1987

• Skytron Elite Surgical Tables

  Class II

  FDA 510(k) K811311 Active Cleared 2 Jun 1981

See all devices from Skytron, Div. the Kmw Group, Inc. →