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FDA 510(k)

TECHNICARE MODEL 1047

K-Number: K840390 · 1984-02-21

ApplicantTechnicare Corp.
Decision Date1984-02-21
Product CodeJAA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

TECHNICARE MODEL 1047 is the device name listed in this FDA 510(k) record. The listed applicant is Technicare Corp.. It received FDA 510(k) clearance on 1984-02-21 under 510(k) number K840390. The device is classified under product code JAA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TECHNICARE MODEL 1047?

TECHNICARE MODEL 1047 is a medical device that received FDA 510(k) clearance on 1984-02-21. The listed applicant is Technicare Corp.. The 510(k) number is K840390.

When did TECHNICARE MODEL 1047 receive FDA 510(k) clearance?

TECHNICARE MODEL 1047 received FDA 510(k) clearance on 1984-02-21, under 510(k) number K840390.

Who is the listed applicant for TECHNICARE MODEL 1047?

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

What is the FDA product code for TECHNICARE MODEL 1047?

The FDA product code for TECHNICARE MODEL 1047 is JAA.

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Other records listing Technicare Corp. as applicant

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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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