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FDA 510(k)

PMT VAXIOM STEREOTACTIC SYS #FX001

K-Number: K831329 · 1983-06-15

ApplicantProgress Mankind Technology
Decision Date1983-06-15
Product CodeHAW
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

PMT VAXIOM STEREOTACTIC SYS #FX001 is the device name listed in this FDA 510(k) record. The listed applicant is Progress Mankind Technology. It received FDA 510(k) clearance on 1983-06-15 under 510(k) number K831329. The device is classified under product code HAW. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PMT VAXIOM STEREOTACTIC SYS #FX001?

PMT VAXIOM STEREOTACTIC SYS #FX001 is a medical device that received FDA 510(k) clearance on 1983-06-15. The listed applicant is Progress Mankind Technology. The 510(k) number is K831329.

When did PMT VAXIOM STEREOTACTIC SYS #FX001 receive FDA 510(k) clearance?

PMT VAXIOM STEREOTACTIC SYS #FX001 received FDA 510(k) clearance on 1983-06-15, under 510(k) number K831329.

Who is the listed applicant for PMT VAXIOM STEREOTACTIC SYS #FX001?

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

What is the FDA product code for PMT VAXIOM STEREOTACTIC SYS #FX001?

The FDA product code for PMT VAXIOM STEREOTACTIC SYS #FX001 is HAW.

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Other records listing Progress Mankind Technology 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.

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Related Devices (Code: HAW)

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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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