FDA 510(k)

LPA-1 PRESSURE MONITOR

K-Number: K854022 · 1985-12-24

Decision Date1985-12-24

Product Code

DecisionSubstantially Equivalent

Device Summary

LPA-1 PRESSURE MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Life Products, Inc.. It received FDA 510(k) clearance on 1985-12-24 under 510(k) number K854022. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LPA-1 PRESSURE MONITOR?

LPA-1 PRESSURE MONITOR is a medical device that received FDA 510(k) clearance on 1985-12-24. The listed applicant is Life Products, Inc.. The 510(k) number is K854022.

When did LPA-1 PRESSURE MONITOR receive FDA 510(k) clearance?

LPA-1 PRESSURE MONITOR received FDA 510(k) clearance on 1985-12-24, under 510(k) number K854022.

Who is the listed applicant for LPA-1 PRESSURE MONITOR?

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

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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.