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FDA 510(k)

DIGITAL FLUOROGRAPHIC IMAGING SYSTEM DIGIFORMER

K-Number: K844037 · 1985-03-01

ApplicantToshiba Medical Systems
Decision Date1985-03-01
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DIGITAL FLUOROGRAPHIC IMAGING SYSTEM DIGIFORMER 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 1985-03-01 under 510(k) number K844037. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIGITAL FLUOROGRAPHIC IMAGING SYSTEM DIGIFORMER?

DIGITAL FLUOROGRAPHIC IMAGING SYSTEM DIGIFORMER is a medical device that received FDA 510(k) clearance on 1985-03-01. The listed applicant is Toshiba Medical Systems. The 510(k) number is K844037.

When did DIGITAL FLUOROGRAPHIC IMAGING SYSTEM DIGIFORMER receive FDA 510(k) clearance?

DIGITAL FLUOROGRAPHIC IMAGING SYSTEM DIGIFORMER received FDA 510(k) clearance on 1985-03-01, under 510(k) number K844037.

Who is the listed applicant for DIGITAL FLUOROGRAPHIC IMAGING SYSTEM DIGIFORMER?

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 DIGITAL FLUOROGRAPHIC IMAGING SYSTEM DIGIFORMER?

The FDA product code for DIGITAL FLUOROGRAPHIC IMAGING SYSTEM DIGIFORMER is LLZ.

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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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