Heel or Elbow Protector

FDA 510(k) K812344 · Fred Sammons, Inc.

Substantially Equivalent

510(k) numberK812344

Submission

Device name
Heel or Elbow Protector
Applicant
Fred Sammons, Inc.
Mchenry, IL, US
Received
August 18, 1981
Decision date
September 11, 1981
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

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K820584Decubicare Pads & AccessoriesFMP · Traditional Abco Dealers, Inc.03/25/1982SE
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

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Questions and answers

When was Heel or Elbow Protector cleared by the FDA?

Heel or Elbow Protector (K812344) received a 510(k) decision of Substantially Equivalent on September 11, 1981, 24 days after the submission was received.

What is the product code of K812344?

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