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FDA 510(k)

JAGUAR

K-Number: K852809 · 1985-08-22

ApplicantInacare Corp.
Decision Date1985-08-22
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

JAGUAR is the device name listed in this FDA 510(k) record. The listed applicant is Inacare Corp.. It received FDA 510(k) clearance on 1985-08-22 under 510(k) number K852809. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JAGUAR?

JAGUAR is a medical device that received FDA 510(k) clearance on 1985-08-22. The listed applicant is Inacare Corp.. The 510(k) number is K852809.

When did JAGUAR receive FDA 510(k) clearance?

JAGUAR received FDA 510(k) clearance on 1985-08-22, under 510(k) number K852809.

Who is the listed applicant for JAGUAR?

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

What is the FDA product code for JAGUAR?

The FDA product code for JAGUAR is ITI.

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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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