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FDA 510(k)

G5 APPARATUS T, K1, K3 & THE PRESIDENT MODEL'S

K-Number: K850851 · 1985-06-25

ApplicantPhysio Technology, Inc.
Decision Date1985-06-25
Product CodeISA
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

G5 APPARATUS T, K1, K3 & THE PRESIDENT MODEL'S is the device name listed in this FDA 510(k) record. The listed applicant is Physio Technology, Inc.. It received FDA 510(k) clearance on 1985-06-25 under 510(k) number K850851. The device is classified under product code ISA. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the G5 APPARATUS T, K1, K3 & THE PRESIDENT MODEL'S?

G5 APPARATUS T, K1, K3 & THE PRESIDENT MODEL'S is a medical device that received FDA 510(k) clearance on 1985-06-25. The listed applicant is Physio Technology, Inc.. The 510(k) number is K850851.

When did G5 APPARATUS T, K1, K3 & THE PRESIDENT MODEL'S receive FDA 510(k) clearance?

G5 APPARATUS T, K1, K3 & THE PRESIDENT MODEL'S received FDA 510(k) clearance on 1985-06-25, under 510(k) number K850851.

Who is the listed applicant for G5 APPARATUS T, K1, K3 & THE PRESIDENT MODEL'S?

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

What is the FDA product code for G5 APPARATUS T, K1, K3 & THE PRESIDENT MODEL'S?

The FDA product code for G5 APPARATUS T, K1, K3 & THE PRESIDENT MODEL'S is ISA.

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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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