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FDA 510(k)

PRACTICE PARTNER

K-Number: K926315 · 1993-12-13

ApplicantRs Imaging
Decision Date1993-12-13
Product CodeLMD
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PRACTICE PARTNER is the device name listed in this FDA 510(k) record. The listed applicant is Rs Imaging. It received FDA 510(k) clearance on 1993-12-13 under 510(k) number K926315. The device is classified under product code LMD. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRACTICE PARTNER?

PRACTICE PARTNER is a medical device that received FDA 510(k) clearance on 1993-12-13. The listed applicant is Rs Imaging. The 510(k) number is K926315.

When did PRACTICE PARTNER receive FDA 510(k) clearance?

PRACTICE PARTNER received FDA 510(k) clearance on 1993-12-13, under 510(k) number K926315.

Who is the listed applicant for PRACTICE PARTNER?

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

What is the FDA product code for PRACTICE PARTNER?

The FDA product code for PRACTICE PARTNER is LMD.

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Official Source

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

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