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FDA 510(k)

LPA-2 REMOTE ALARM

K-Number: K851905 · 1985-07-08

ApplicantLife Products, Inc.
Decision Date1985-07-08
Product CodeCAP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LPA-2 REMOTE ALARM 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 1985-07-08 under 510(k) number K851905. The device is classified under product code CAP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LPA-2 REMOTE ALARM?

LPA-2 REMOTE ALARM is a medical device that received FDA 510(k) clearance on 1985-07-08. The listed applicant is Life Products, Inc.. The 510(k) number is K851905.

When did LPA-2 REMOTE ALARM receive FDA 510(k) clearance?

LPA-2 REMOTE ALARM received FDA 510(k) clearance on 1985-07-08, under 510(k) number K851905.

Who is the listed applicant for LPA-2 REMOTE ALARM?

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

What is the FDA product code for LPA-2 REMOTE ALARM?

The FDA product code for LPA-2 REMOTE ALARM is CAP.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Life Products, 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.

K901714LIFESTYLE HOME TANNING UNITSK854022LPA-1 PRESSURE MONITORK850151L100B UNIVERSAL & L100A NIGHT PATIENT CIRCUITK851805LPA-3 PRINTERK844179LP-5K8421224A

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Related Devices (Code: CAP)

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.

K201666SINGLE USE MANOMETERFlexicare Medical Limited.K182292VORTRAN APM-PlusVortran Medical Technology 1, Inc.K180510NS 120P-TRS Airway Pressure GaugeInstrumentation Industries, Inc.K172284NAPA LP-15 Airway Pressure MonitorDrw Medical, LLCK153733VORTRAN ManometerVortran Medical Technology 1, Inc.K122627GIO DIGITAL PRESSURE GUAGESGalemed Corp.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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