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FDA 510(k)

TIGERSCAN/TIGERVIEW

K-Number: K955237 · 1996-04-04

ApplicantTau Corp.
Decision Date1996-04-04
Product CodeLMB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

TIGERSCAN/TIGERVIEW is the device name listed in this FDA 510(k) record. The listed applicant is Tau Corp.. It received FDA 510(k) clearance on 1996-04-04 under 510(k) number K955237. The device is classified under product code LMB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TIGERSCAN/TIGERVIEW?

TIGERSCAN/TIGERVIEW is a medical device that received FDA 510(k) clearance on 1996-04-04. The listed applicant is Tau Corp.. The 510(k) number is K955237.

When did TIGERSCAN/TIGERVIEW receive FDA 510(k) clearance?

TIGERSCAN/TIGERVIEW received FDA 510(k) clearance on 1996-04-04, under 510(k) number K955237.

Who is the listed applicant for TIGERSCAN/TIGERVIEW?

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

What is the FDA product code for TIGERSCAN/TIGERVIEW?

The FDA product code for TIGERSCAN/TIGERVIEW is LMB.

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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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