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FDA 510(k)

PAM PLUS

K-Number: K913998 · 1992-01-08

ApplicantKinetic Concepts, Inc.
Decision Date1992-01-08
Product CodeIRO
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PAM PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Kinetic Concepts, Inc.. It received FDA 510(k) clearance on 1992-01-08 under 510(k) number K913998. The device is classified under product code IRO. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PAM PLUS?

PAM PLUS is a medical device that received FDA 510(k) clearance on 1992-01-08. The listed applicant is Kinetic Concepts, Inc.. The 510(k) number is K913998.

When did PAM PLUS receive FDA 510(k) clearance?

PAM PLUS received FDA 510(k) clearance on 1992-01-08, under 510(k) number K913998.

Who is the listed applicant for PAM PLUS?

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

What is the FDA product code for PAM PLUS?

The FDA product code for PAM PLUS is IRO.

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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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