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FDA 510(k)

REDI-VU MODEL RV-386

K-Number: K890397 · 1989-04-14

ApplicantJ.D. Technical Services
Decision Date1989-04-14
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

REDI-VU MODEL RV-386 is the device name listed in this FDA 510(k) record. The listed applicant is J.D. Technical Services. It received FDA 510(k) clearance on 1989-04-14 under 510(k) number K890397. 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 REDI-VU MODEL RV-386?

REDI-VU MODEL RV-386 is a medical device that received FDA 510(k) clearance on 1989-04-14. The listed applicant is J.D. Technical Services. The 510(k) number is K890397.

When did REDI-VU MODEL RV-386 receive FDA 510(k) clearance?

REDI-VU MODEL RV-386 received FDA 510(k) clearance on 1989-04-14, under 510(k) number K890397.

Who is the listed applicant for REDI-VU MODEL RV-386?

The FDA 510(k) record lists J.D. Technical Services as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for REDI-VU MODEL RV-386?

The FDA product code for REDI-VU MODEL RV-386 is LLZ.

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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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