Specimen Collection & Transport System

FDA 510(k) K844475 · Portable Medical Laboratories, Inc.

Substantially Equivalent

510(k) numberK844475

Submission

Device name
Specimen Collection & Transport System
Applicant
Portable Medical Laboratories, Inc.
Solana Beach, CA, US
Received
November 19, 1984
Decision date
February 6, 1985
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
FMF – Syringe, Piston
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5860
Specialty
General Hospital

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More from Instylla, Inc.

510(k)DeviceDecision
K882101Hemoglobin Screening DeviceKSL · Traditional 07/01/1988SE
K874190Cell Counting Grid GraticuleIBJ · Traditional 01/05/1988SE
K871671Urinoscopy FunnelGHO · Traditional 05/20/1987SE
K864049Mcarthur Microscope, Standard Metal VersionIBJ · Traditional 10/29/1986SE
K854735Mcarthur Microscope Plastic Version with Acc.IBJ · Traditional 12/10/1985SE
K844476Portable Diagnostic LaboratoryLIB · Traditional 03/13/1985SE
K844442Rapid Diagnostic KitLIB · Traditional 02/01/1985SE
K844473Hand-Held Slide ReaderLIB · Traditional 01/04/1985SE

Questions and answers

When was Specimen Collection & Transport System cleared by the FDA?

Specimen Collection & Transport System (K844475) received a 510(k) decision of Substantially Equivalent on February 6, 1985, 79 days after the submission was received.

What is the product code of K844475?

The FDA product code is FMF – Syringe, Piston, a Class II (moderate risk) device regulated under 21 CFR 880.5860.