Mtp Disposable Equipment Covers, Karl Storz 15 Touch Screen

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K091178 ↗

FDA Product Code

MMP

Device Class

Class II

Regulation

21 CFR Part 878.4370

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

• Mtp Disposable Trocars

  Class II

  FDA 510(k) K994066 Active Cleared 20 Jan 2000

• Mtp Extraction Bag

  Class II

  FDA 510(k) K990912 Active Cleared 9 Jun 1999

• Mtp Hamou Endomat Disposable Tubing Sets

  Class II

  FDA 510(k) K990910 Active Cleared 3 Jun 1999

• Mtp Laparomat Disposable Tubing Set

  Class II

  FDA 510(k) K011360 Active Cleared 19 Jul 2001

• Mtp Disposable Trocar Valves

  Class II

  FDA 510(k) K000337 Active Cleared 12 Apr 2000

• Mtp Uropump Disposable Tubing Set

  Class II

  FDA 510(k) K990909 Active Cleared 9 Jun 1999

See all devices from Mtp Medical Technical Promotion GmbH →