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FDA 510(k)

L.O.N. PRES MON LINES, CPC LINES, ADMINISTRATION

K-Number: K853099 · 1985-12-03

ApplicantL.O.N. Research, Inc.
Decision Date1985-12-03
Product CodeDTL
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

L.O.N. PRES MON LINES, CPC LINES, ADMINISTRATION is the device name listed in this FDA 510(k) record. The listed applicant is L.O.N. Research, Inc.. It received FDA 510(k) clearance on 1985-12-03 under 510(k) number K853099. The device is classified under product code DTL. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the L.O.N. PRES MON LINES, CPC LINES, ADMINISTRATION?

L.O.N. PRES MON LINES, CPC LINES, ADMINISTRATION is a medical device that received FDA 510(k) clearance on 1985-12-03. The listed applicant is L.O.N. Research, Inc.. The 510(k) number is K853099.

When did L.O.N. PRES MON LINES, CPC LINES, ADMINISTRATION receive FDA 510(k) clearance?

L.O.N. PRES MON LINES, CPC LINES, ADMINISTRATION received FDA 510(k) clearance on 1985-12-03, under 510(k) number K853099.

Who is the listed applicant for L.O.N. PRES MON LINES, CPC LINES, ADMINISTRATION?

The FDA 510(k) record lists L.O.N. Research, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for L.O.N. PRES MON LINES, CPC LINES, ADMINISTRATION?

The FDA product code for L.O.N. PRES MON LINES, CPC LINES, ADMINISTRATION is DTL.

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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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