FDA 510(k)

ANU-RX

K-Number: K862490 · 1986-08-18

Decision Date1986-08-18

Product CodeLKX

DecisionSubstantially Equivalent

Device Summary

ANU-RX is the device name listed in this FDA 510(k) record. The listed applicant is J. & Jp., Inc.. It received FDA 510(k) clearance on 1986-08-18 under 510(k) number K862490. The device is classified under product code LKX. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANU-RX?

ANU-RX is a medical device that received FDA 510(k) clearance on 1986-08-18. The listed applicant is J. & Jp., Inc.. The 510(k) number is K862490.

When did ANU-RX receive FDA 510(k) clearance?

ANU-RX received FDA 510(k) clearance on 1986-08-18, under 510(k) number K862490.

Who is the listed applicant for ANU-RX?

The FDA 510(k) record lists J. & Jp., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ANU-RX?

The FDA product code for ANU-RX is LKX.

Other records listing J. & Jp., Inc. as applicant

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.

K852679MULTIPLE(HEMORX) IF APPROVED BY TRADEMARK OFFICE

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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.