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FDA 510(k)

TISSU TRANS FILTRON, MODELS 3-TT-FILTRON 2000-500

K-Number: K092482 · 2009-12-04

ApplicantShippert Medical Technologies Corp.
Decision Date2009-12-04
Product CodeMUU
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TISSU TRANS FILTRON, MODELS 3-TT-FILTRON 2000-500 is the device name listed in this FDA 510(k) record. The listed applicant is Shippert Medical Technologies Corp.. It received FDA 510(k) clearance on 2009-12-04 under 510(k) number K092482. The device is classified under product code MUU. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TISSU TRANS FILTRON, MODELS 3-TT-FILTRON 2000-500?

TISSU TRANS FILTRON, MODELS 3-TT-FILTRON 2000-500 is a medical device that received FDA 510(k) clearance on 2009-12-04. The listed applicant is Shippert Medical Technologies Corp.. The 510(k) number is K092482.

When did TISSU TRANS FILTRON, MODELS 3-TT-FILTRON 2000-500 receive FDA 510(k) clearance?

TISSU TRANS FILTRON, MODELS 3-TT-FILTRON 2000-500 received FDA 510(k) clearance on 2009-12-04, under 510(k) number K092482.

Who is the listed applicant for TISSU TRANS FILTRON, MODELS 3-TT-FILTRON 2000-500?

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

What is the FDA product code for TISSU TRANS FILTRON, MODELS 3-TT-FILTRON 2000-500?

The FDA product code for TISSU TRANS FILTRON, MODELS 3-TT-FILTRON 2000-500 is MUU.

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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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