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FDA 510(k)

TP440 ORTHOPROBE

K-Number: K821571 · 1982-07-21

ApplicantGrove Video Corp.
Decision Date1982-07-21
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

TP440 ORTHOPROBE is the device name listed in this FDA 510(k) record. The listed applicant is Grove Video Corp.. It received FDA 510(k) clearance on 1982-07-21 under 510(k) number K821571. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TP440 ORTHOPROBE?

TP440 ORTHOPROBE is a medical device that received FDA 510(k) clearance on 1982-07-21. The listed applicant is Grove Video Corp.. The 510(k) number is K821571.

When did TP440 ORTHOPROBE receive FDA 510(k) clearance?

TP440 ORTHOPROBE received FDA 510(k) clearance on 1982-07-21, under 510(k) number K821571.

Who is the listed applicant for TP440 ORTHOPROBE?

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

What is the FDA product code for TP440 ORTHOPROBE?

The FDA product code for TP440 ORTHOPROBE is GZJ.

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Related Devices (Code: GZJ)

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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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