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FDA 510(k)

MASSAGER

K-Number: K944730 · 1995-02-14

ApplicantNorth American Technical Services Corp.
Decision Date1995-02-14
Product CodeISA
Advisory CommitteePM
DecisionSubstantially Equivalent for Some Indications

Device Summary

MASSAGER is the device name listed in this FDA 510(k) record. The listed applicant is North American Technical Services Corp.. It received FDA 510(k) clearance on 1995-02-14 under 510(k) number K944730. The device is classified under product code ISA. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the MASSAGER?

MASSAGER is a medical device that received FDA 510(k) clearance on 1995-02-14. The listed applicant is North American Technical Services Corp.. The 510(k) number is K944730.

When did MASSAGER receive FDA 510(k) clearance?

MASSAGER received FDA 510(k) clearance on 1995-02-14, under 510(k) number K944730.

Who is the listed applicant for MASSAGER?

The FDA 510(k) record lists North American Technical Services Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MASSAGER?

The FDA product code for MASSAGER is ISA.

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Other records listing North American Technical Services Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: 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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