Conphar, Tuning Forks

FDA 510(k) K813304 · Conphar, Inc.

Substantially Equivalent

510(k) numberK813304

Submission

Device name
Conphar, Tuning Forks
Applicant
Conphar, Inc.
Mchenry, IL, US
Received
November 23, 1981
Decision date
December 10, 1981
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
GWX – Fork, Tuning
Device class
Class I (low risk)
Regulation
21 CFR 882.1525
Specialty
Neurology

Other 510(k)s with product code GWX

510(k)DeviceApplicantDecision
K874966Tuning ForksGWX · Traditional Solway, Inc.01/04/1988SE
K761132Tuning ForkGWX · Traditional Fred Sammons, Inc.12/02/1976SE
K760303Fork, Tuning BK-7519GWX · Traditional Fred Sammons, Inc.09/08/1976SE

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K821289Mayo-Hegar Needle HolderGDF · Traditional 06/03/1982SE
K821298Backhaus Clamp, 3 1/2HTD · Traditional 05/28/1982SE
K821294Tonsil Scissors Straight 5 1/2EGN · Traditional 05/28/1982SE
K821293Backhaus Clamp, 5 1/4HTD · Traditional 05/28/1982SE
K821292Tonsil Scissors 7EGN · Traditional 05/28/1982SE
K821290Littauer Scissors 5 1/2HNF · Traditional 05/28/1982SE
K821286Iris Scissors Straight 4 1/2HNF · Traditional 05/28/1982SE

Questions and answers

When was Conphar, Tuning Forks cleared by the FDA?

Conphar, Tuning Forks (K813304) received a 510(k) decision of Substantially Equivalent on December 10, 1981, 17 days after the submission was received.

What is the product code of K813304?

The FDA product code is GWX – Fork, Tuning, a Class I (low risk) device regulated under 21 CFR 882.1525.