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FDA 510(k)

TUBESTAND MODEL DS-TA-4

K-Number: K771297 · 1977-08-03

ApplicantToshiba Medical Systems
Decision Date1977-08-03
Product CodeIZF
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

TUBESTAND MODEL DS-TA-4 is the device name listed in this FDA 510(k) record. The listed applicant is Toshiba Medical Systems. It received FDA 510(k) clearance on 1977-08-03 under 510(k) number K771297. The device is classified under product code IZF. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TUBESTAND MODEL DS-TA-4?

TUBESTAND MODEL DS-TA-4 is a medical device that received FDA 510(k) clearance on 1977-08-03. The listed applicant is Toshiba Medical Systems. The 510(k) number is K771297.

When did TUBESTAND MODEL DS-TA-4 receive FDA 510(k) clearance?

TUBESTAND MODEL DS-TA-4 received FDA 510(k) clearance on 1977-08-03, under 510(k) number K771297.

Who is the listed applicant for TUBESTAND MODEL DS-TA-4?

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

What is the FDA product code for TUBESTAND MODEL DS-TA-4?

The FDA product code for TUBESTAND MODEL DS-TA-4 is IZF.

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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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