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FDA 510(k)

VITATRON 88

K-Number: K811939 · 1981-07-23

ApplicantVitatronics
Decision Date1981-07-23
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

VITATRON 88 is the device name listed in this FDA 510(k) record. The listed applicant is Vitatronics. It received FDA 510(k) clearance on 1981-07-23 under 510(k) number K811939. 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 VITATRON 88?

VITATRON 88 is a medical device that received FDA 510(k) clearance on 1981-07-23. The listed applicant is Vitatronics. The 510(k) number is K811939.

When did VITATRON 88 receive FDA 510(k) clearance?

VITATRON 88 received FDA 510(k) clearance on 1981-07-23, under 510(k) number K811939.

Who is the listed applicant for VITATRON 88?

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

What is the FDA product code for VITATRON 88?

The FDA product code for VITATRON 88 is GZJ.

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Related Devices (Code: GZJ)

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

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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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