Arterial Blood Sampling Kit

FDA 510(k) K802185 · Current Technologies, Inc.

Substantially Equivalent

510(k) numberK802185

Submission

Device name
Arterial Blood Sampling Kit
Applicant
Current Technologies, Inc.
Mchenry, IL, US
Received
September 10, 1980
Decision date
October 10, 1980
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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
K150243Invictus Medical GelShieldFMP · Traditional Invictus Medical, Inc.05/01/2015SE
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
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

More from American Hospital Supply Corp.

510(k)DeviceDecision
K833312Arterial Micro Collection KitJKA · Traditional 12/08/1983SE
K810816Prefilled Arterial Blood Sampling SyringJKA · Traditional 04/07/1981SE

Questions and answers

When was Arterial Blood Sampling Kit cleared by the FDA?

Arterial Blood Sampling Kit (K802185) received a 510(k) decision of Substantially Equivalent on October 10, 1980, 30 days after the submission was received.

What is the product code of K802185?

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