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FDA 510(k)

TECHNICARE 280

K-Number: K834486 · 1984-04-13

ApplicantTechnicare Corp.
Decision Date1984-04-13
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

TECHNICARE 280 is the device name listed in this FDA 510(k) record. The listed applicant is Technicare Corp.. It received FDA 510(k) clearance on 1984-04-13 under 510(k) number K834486. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TECHNICARE 280?

TECHNICARE 280 is a medical device that received FDA 510(k) clearance on 1984-04-13. The listed applicant is Technicare Corp.. The 510(k) number is K834486.

When did TECHNICARE 280 receive FDA 510(k) clearance?

TECHNICARE 280 received FDA 510(k) clearance on 1984-04-13, under 510(k) number K834486.

Who is the listed applicant for TECHNICARE 280?

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 280?

The FDA product code for TECHNICARE 280 is IYO.

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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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