Invictus Medical GelShield

FDA 510(k) K150243 · Invictus Medical, Inc.

Substantially Equivalent

510(k) numberK150243

Submission

Device name
Invictus Medical GelShield
Applicant
Invictus Medical, Inc.
San Antonio, TX, US
Received
February 2, 2015
Decision date
May 1, 2015
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FMP – Protector, Skin Pressure
Device class
Class I (low risk)
Regulation
21 CFR 880.6450
Specialty
General Hospital

Other 510(k)s with product code FMP

510(k)DeviceApplicantDecision
K951325Comfeel Plus Pressure Relief DressingFMP · Traditional Richard Hamer Assoc., Inc.07/31/1995SE
K934731Medsurg Sterile Imaging ProductsFMP · Traditional Medsurg Industries, Inc.03/28/1994SE
K820584Decubicare Pads & AccessoriesFMP · Traditional Abco Dealers, Inc.03/25/1982SE
K812344Heel or Elbow ProtectorFMP · Traditional Fred Sammons, Inc.09/11/1981SE
K811184Spenco Dermal PadsFMP · Traditional Spenco Medical Corp.05/20/1981SE
K802829Scanlan Vascu-StattFMP · Traditional Scanlan Intl., Inc.01/15/1981SE
K802185Arterial Blood Sampling KitFMP · Traditional Current Technologies, Inc.10/10/1980SE
K801694Flotation Pad for Operating TableFMP · Traditional Action Products, Inc.08/27/1980SE
K801195Dermalex or Natrawool Skin Pressure ProtFMP · Traditional Stock Wild & Co.06/09/1980SE
K792297Span Aids KitFMP · Traditional American Hospital Supply Corp.12/20/1979SE

Questions and answers

When was Invictus Medical GelShield cleared by the FDA?

Invictus Medical GelShield (K150243) received a 510(k) decision of Substantially Equivalent on May 1, 2015, 88 days after the submission was received.

What is the product code of K150243?

The FDA product code is FMP – Protector, Skin Pressure, a Class I (low risk) device regulated under 21 CFR 880.6450.