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FDA 510(k)

INVACARE 3G TARSYS

K-Number: K033819 · 2004-06-04

ApplicantInvacare Corp.
Decision Date2004-06-04
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

INVACARE 3G TARSYS is the device name listed in this FDA 510(k) record. The listed applicant is Invacare Corp.. It received FDA 510(k) clearance on 2004-06-04 under 510(k) number K033819. 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 INVACARE 3G TARSYS?

INVACARE 3G TARSYS is a medical device that received FDA 510(k) clearance on 2004-06-04. The listed applicant is Invacare Corp.. The 510(k) number is K033819.

When did INVACARE 3G TARSYS receive FDA 510(k) clearance?

INVACARE 3G TARSYS received FDA 510(k) clearance on 2004-06-04, under 510(k) number K033819.

Who is the listed applicant for INVACARE 3G TARSYS?

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

What is the FDA product code for INVACARE 3G TARSYS?

The FDA product code for INVACARE 3G TARSYS is ITI.

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Other records listing Invacare 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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