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FDA 510(k)

PLANMED VERITY

K-Number: K121418 · 2013-02-01

ApplicantPlanmed OY
Decision Date2013-02-01
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PLANMED VERITY is the device name listed in this FDA 510(k) record. The listed applicant is Planmed OY. It received FDA 510(k) clearance on 2013-02-01 under 510(k) number K121418. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PLANMED VERITY?

PLANMED VERITY is a medical device that received FDA 510(k) clearance on 2013-02-01. The listed applicant is Planmed OY. The 510(k) number is K121418.

When did PLANMED VERITY receive FDA 510(k) clearance?

PLANMED VERITY received FDA 510(k) clearance on 2013-02-01, under 510(k) number K121418.

Who is the listed applicant for PLANMED VERITY?

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

What is the FDA product code for PLANMED VERITY?

The FDA product code for PLANMED VERITY is JAK.

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Other records listing Planmed OY as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K250318Planmed XFIK211720Planmed Clarity 2D, Planmed Clarify SK213278Planmed VerityK192317Planmed Clarity 2D and Clarity SK180918Planmed VerityK163328Planmed Clarity

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Related Devices (Code: JAK)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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