Synovialscopics, Synovial Fluid Control

FDA 510(k) K010598 · Quantimetrix Corp.

Substantially Equivalent

510(k) numberK010598

Submission

Device name
Synovialscopics, Synovial Fluid Control
Applicant
Quantimetrix Corp.
Redondo Beach, CA, US
Received
February 28, 2001
Decision date
March 23, 2001
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
JPK – Mixture, Hematology Quality Control
Device class
Class II (moderate risk)
Regulation
21 CFR 864.8625
Specialty
Hematology

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Questions and answers

When was Synovialscopics, Synovial Fluid Control cleared by the FDA?

Synovialscopics, Synovial Fluid Control (K010598) received a 510(k) decision of Substantially Equivalent on March 23, 2001, 23 days after the submission was received.

What is the product code of K010598?

The FDA product code is JPK – Mixture, Hematology Quality Control, a Class II (moderate risk) device regulated under 21 CFR 864.8625.