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FDA 510(k)

POLYSONIC ULTRASOUND LOTION

K-Number: K827296 · 1982-04-16

ApplicantParker Laboratories, Inc.
Decision Date1982-04-16
Product CodeMUI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

POLYSONIC ULTRASOUND LOTION is the device name listed in this FDA 510(k) record. The listed applicant is Parker Laboratories, Inc.. It received FDA 510(k) clearance on 1982-04-16 under 510(k) number K827296. The device is classified under product code MUI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POLYSONIC ULTRASOUND LOTION?

POLYSONIC ULTRASOUND LOTION is a medical device that received FDA 510(k) clearance on 1982-04-16. The listed applicant is Parker Laboratories, Inc.. The 510(k) number is K827296.

When did POLYSONIC ULTRASOUND LOTION receive FDA 510(k) clearance?

POLYSONIC ULTRASOUND LOTION received FDA 510(k) clearance on 1982-04-16, under 510(k) number K827296.

Who is the listed applicant for POLYSONIC ULTRASOUND LOTION?

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

What is the FDA product code for POLYSONIC ULTRASOUND LOTION?

The FDA product code for POLYSONIC ULTRASOUND LOTION is MUI.

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Other records listing Parker Laboratories, Inc. as applicant

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Related Devices (Code: MUI)

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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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