Pathfinder(Tm) Specimen Collection Kit

FDA 510(k) K863682 · Kallestad Laboratories, Inc.

Substantially Equivalent

510(k) numberK863682

Submission

Device name
Pathfinder(Tm) Specimen Collection Kit
Applicant
Kallestad Laboratories, Inc.
Chaska, MN, US
Received
September 19, 1986
Decision date
October 10, 1986
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JSM – Culture Media, Non-Propagating Transport
Device class
Class I (low risk)
Regulation
21 CFR 866.2390
Specialty
Microbiology

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K862313Kallestad Sm/Rnp Test ReagentLKJ · Traditional 08/06/1986SE
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K855014Quantimetric Plus Calibrator/Control Set aJIX · Traditional 03/14/1986SE
K855010Quantimetric Plus Igm Reagent KitDFT · Traditional 02/28/1986SE
K855013Quantimetric Plus Support PackDEH · Traditional 02/26/1986SE
K855012Quantimetric Plus C4 Reagent KitDBI · Traditional 02/26/1986SE
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Questions and answers

When was Pathfinder(Tm) Specimen Collection Kit cleared by the FDA?

Pathfinder(Tm) Specimen Collection Kit (K863682) received a 510(k) decision of Substantially Equivalent on October 10, 1986, 21 days after the submission was received.

What is the product code of K863682?

The FDA product code is JSM – Culture Media, Non-Propagating Transport, a Class I (low risk) device regulated under 21 CFR 866.2390.