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FDA 510(k)

PROPIOCEPTOR MASSAGER

K-Number: K760616 · 1977-01-13

ApplicantCellers Research, Inc.
Decision Date1977-01-13
Product CodeISA
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PROPIOCEPTOR MASSAGER is the device name listed in this FDA 510(k) record. The listed applicant is Cellers Research, Inc.. It received FDA 510(k) clearance on 1977-01-13 under 510(k) number K760616. 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 PROPIOCEPTOR MASSAGER?

PROPIOCEPTOR MASSAGER is a medical device that received FDA 510(k) clearance on 1977-01-13. The listed applicant is Cellers Research, Inc.. The 510(k) number is K760616.

When did PROPIOCEPTOR MASSAGER receive FDA 510(k) clearance?

PROPIOCEPTOR MASSAGER received FDA 510(k) clearance on 1977-01-13, under 510(k) number K760616.

Who is the listed applicant for PROPIOCEPTOR MASSAGER?

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

What is the FDA product code for PROPIOCEPTOR MASSAGER?

The FDA product code for PROPIOCEPTOR MASSAGER is ISA.

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Related Devices (Code: ISA)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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