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FDA 510(k)

TUBE CONVEYOR MODEL DS-PB-4

K-Number: K771296 · 1977-08-03

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

Device Summary

TUBE CONVEYOR MODEL DS-PB-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 K771296. 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 TUBE CONVEYOR MODEL DS-PB-4?

TUBE CONVEYOR MODEL DS-PB-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 K771296.

When did TUBE CONVEYOR MODEL DS-PB-4 receive FDA 510(k) clearance?

TUBE CONVEYOR MODEL DS-PB-4 received FDA 510(k) clearance on 1977-08-03, under 510(k) number K771296.

Who is the listed applicant for TUBE CONVEYOR MODEL DS-PB-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 TUBE CONVEYOR MODEL DS-PB-4?

The FDA product code for TUBE CONVEYOR MODEL DS-PB-4 is IZF.

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Other records listing Toshiba Medical Systems as applicant

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K960948SCATTER CORRECTION VOLUME SOFTWARE MODEL NSSC-020AK954310BLA-800AK954309ANGIOREXK893750MRT-50A MOBILEK891453DIAGNOSTIC ULTRASOUND TRANSDUCER: PVE-582VK890969TRANSESOPHAGEAL TRANSDUCER PEF-511SA

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Related Devices (Code: 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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