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FDA 510(k)

TRUVEL TZ-3X X-RAY DIGITIZING SCANNER

K-Number: K890970 · 1989-05-11

ApplicantTruvel Corp.
Decision Date1989-05-11
Product CodeLMA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

TRUVEL TZ-3X X-RAY DIGITIZING SCANNER is the device name listed in this FDA 510(k) record. The listed applicant is Truvel Corp.. It received FDA 510(k) clearance on 1989-05-11 under 510(k) number K890970. The device is classified under product code LMA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRUVEL TZ-3X X-RAY DIGITIZING SCANNER?

TRUVEL TZ-3X X-RAY DIGITIZING SCANNER is a medical device that received FDA 510(k) clearance on 1989-05-11. The listed applicant is Truvel Corp.. The 510(k) number is K890970.

When did TRUVEL TZ-3X X-RAY DIGITIZING SCANNER receive FDA 510(k) clearance?

TRUVEL TZ-3X X-RAY DIGITIZING SCANNER received FDA 510(k) clearance on 1989-05-11, under 510(k) number K890970.

Who is the listed applicant for TRUVEL TZ-3X X-RAY DIGITIZING SCANNER?

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

What is the FDA product code for TRUVEL TZ-3X X-RAY DIGITIZING SCANNER?

The FDA product code for TRUVEL TZ-3X X-RAY DIGITIZING SCANNER is LMA.

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Related Devices (Code: LMA)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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