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FDA 510(k)

TECHNICARE 248 SL & 260SL

K-Number: K841817 · 1984-08-17

ApplicantTechnicare Corp.
Decision Date1984-08-17
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

TECHNICARE 248 SL & 260SL is the device name listed in this FDA 510(k) record. The listed applicant is Technicare Corp.. It received FDA 510(k) clearance on 1984-08-17 under 510(k) number K841817. 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 248 SL & 260SL?

TECHNICARE 248 SL & 260SL is a medical device that received FDA 510(k) clearance on 1984-08-17. The listed applicant is Technicare Corp.. The 510(k) number is K841817.

When did TECHNICARE 248 SL & 260SL receive FDA 510(k) clearance?

TECHNICARE 248 SL & 260SL received FDA 510(k) clearance on 1984-08-17, under 510(k) number K841817.

Who is the listed applicant for TECHNICARE 248 SL & 260SL?

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 248 SL & 260SL?

The FDA product code for TECHNICARE 248 SL & 260SL 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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