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FDA 510(k)

THE SIGNATURE SERIES, MAGNUM 100

K-Number: K934919 · 1994-04-06

ApplicantProgressive Electrical Therapeutics
Decision Date1994-04-06
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

THE SIGNATURE SERIES, MAGNUM 100 is the device name listed in this FDA 510(k) record. The listed applicant is Progressive Electrical Therapeutics. It received FDA 510(k) clearance on 1994-04-06 under 510(k) number K934919. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE SIGNATURE SERIES, MAGNUM 100?

THE SIGNATURE SERIES, MAGNUM 100 is a medical device that received FDA 510(k) clearance on 1994-04-06. The listed applicant is Progressive Electrical Therapeutics. The 510(k) number is K934919.

When did THE SIGNATURE SERIES, MAGNUM 100 receive FDA 510(k) clearance?

THE SIGNATURE SERIES, MAGNUM 100 received FDA 510(k) clearance on 1994-04-06, under 510(k) number K934919.

Who is the listed applicant for THE SIGNATURE SERIES, MAGNUM 100?

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

What is the FDA product code for THE SIGNATURE SERIES, MAGNUM 100?

The FDA product code for THE SIGNATURE SERIES, MAGNUM 100 is IPF.

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Other records listing Progressive Electrical Therapeutics as applicant

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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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