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FDA 510(k)

PMT ACCUPRESSURE INFUSION SYSTEM 3601

K-Number: K854157 · 1986-02-13

ApplicantProgress Mankind Technology
Decision Date1986-02-13
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PMT ACCUPRESSURE INFUSION SYSTEM 3601 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 1986-02-13 under 510(k) number K854157. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PMT ACCUPRESSURE INFUSION SYSTEM 3601?

PMT ACCUPRESSURE INFUSION SYSTEM 3601 is a medical device that received FDA 510(k) clearance on 1986-02-13. The listed applicant is Progress Mankind Technology. The 510(k) number is K854157.

When did PMT ACCUPRESSURE INFUSION SYSTEM 3601 receive FDA 510(k) clearance?

PMT ACCUPRESSURE INFUSION SYSTEM 3601 received FDA 510(k) clearance on 1986-02-13, under 510(k) number K854157.

Who is the listed applicant for PMT ACCUPRESSURE INFUSION SYSTEM 3601?

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 ACCUPRESSURE INFUSION SYSTEM 3601?

The FDA product code for PMT ACCUPRESSURE INFUSION SYSTEM 3601 is FRN.

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Other records listing Progress Mankind Technology as applicant

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Related Devices (Code: FRN)

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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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