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FDA 510(k)

SYNOVIALSCOPICS, SYNOVIAL FLUID CONTROL

K-Number: K010598 · 2001-03-23

ApplicantQuantimetrix Corp.
Decision Date2001-03-23
Product CodeJPK
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

SYNOVIALSCOPICS, SYNOVIAL FLUID CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Quantimetrix Corp.. It received FDA 510(k) clearance on 2001-03-23 under 510(k) number K010598. The device is classified under product code JPK. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYNOVIALSCOPICS, SYNOVIAL FLUID CONTROL?

SYNOVIALSCOPICS, SYNOVIAL FLUID CONTROL is a medical device that received FDA 510(k) clearance on 2001-03-23. The listed applicant is Quantimetrix Corp.. The 510(k) number is K010598.

When did SYNOVIALSCOPICS, SYNOVIAL FLUID CONTROL receive FDA 510(k) clearance?

SYNOVIALSCOPICS, SYNOVIAL FLUID CONTROL received FDA 510(k) clearance on 2001-03-23, under 510(k) number K010598.

Who is the listed applicant for SYNOVIALSCOPICS, SYNOVIAL FLUID CONTROL?

The FDA 510(k) record lists Quantimetrix Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SYNOVIALSCOPICS, SYNOVIAL FLUID CONTROL?

The FDA product code for SYNOVIALSCOPICS, SYNOVIAL FLUID CONTROL is JPK.

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Related Devices (Code: JPK)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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