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FDA 510(k)

CULT-UR

K-Number: K864727 · 1987-01-05

Decision Date1987-01-05
Product CodeLIO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CULT-UR is the device name listed in this FDA 510(k) record. The listed applicant is R.P. Laboratories, Inc.. It received FDA 510(k) clearance on 1987-01-05 under 510(k) number K864727. The device is classified under product code LIO. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CULT-UR?

CULT-UR is a medical device that received FDA 510(k) clearance on 1987-01-05. The listed applicant is R.P. Laboratories, Inc.. The 510(k) number is K864727.

When did CULT-UR receive FDA 510(k) clearance?

CULT-UR received FDA 510(k) clearance on 1987-01-05, under 510(k) number K864727.

Who is the listed applicant for CULT-UR?

The FDA 510(k) record lists R.P. Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CULT-UR?

The FDA product code for CULT-UR is LIO.

Related Devices (Code: LIO)

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.

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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