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FDA 510(k)

LAWRENCE L4000 REFLECTANCE PULSE OXIMETER

K-Number: K874492 · 1988-03-22

ApplicantLawrence Medical Systems, Inc.
Decision Date1988-03-22
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LAWRENCE L4000 REFLECTANCE PULSE OXIMETER is the device name listed in this FDA 510(k) record. The listed applicant is Lawrence Medical Systems, Inc.. It received FDA 510(k) clearance on 1988-03-22 under 510(k) number K874492. The device is classified under product code DQA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LAWRENCE L4000 REFLECTANCE PULSE OXIMETER?

LAWRENCE L4000 REFLECTANCE PULSE OXIMETER is a medical device that received FDA 510(k) clearance on 1988-03-22. The listed applicant is Lawrence Medical Systems, Inc.. The 510(k) number is K874492.

When did LAWRENCE L4000 REFLECTANCE PULSE OXIMETER receive FDA 510(k) clearance?

LAWRENCE L4000 REFLECTANCE PULSE OXIMETER received FDA 510(k) clearance on 1988-03-22, under 510(k) number K874492.

Who is the listed applicant for LAWRENCE L4000 REFLECTANCE PULSE OXIMETER?

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

What is the FDA product code for LAWRENCE L4000 REFLECTANCE PULSE OXIMETER?

The FDA product code for LAWRENCE L4000 REFLECTANCE PULSE OXIMETER is DQA.

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 Lawrence Medical Systems, 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.

K874885LAWRENCE L3000 CARDIAC OUTPUT MONITORK862548TEMPERATURE SENSING ESOPHAGEAL TRANSDUCERK851426ACCUCOM CARDIAC OUTPUT MONITOR

Related Devices (Code: DQA)

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.

K252821Reusable Adult SpO2 Clip Sensor (3m) (M1196A); Reusable Adult SpO2 Clip Sensor (0.9m) (M1196T)Philips Medizin Systeme Böblingen GmbHK252655Pulse Oximeter (PO-A2AO, PO-A2AT, PO-A3AO, PO-H1AO, PO-B1AO, PO-C5AO, PO-C5AT, PO-C6AO, PO-C6AT)Shenzhen Imdk Medical Technology Co., Ltd.K253887Nasal Alar SpO2 Sensor (989803205381); Nasal Alar SpO2 Sensor (989803205391); Nasal Alar Sp02 Sensor (989803205401)Philips Medizin SystemeK260931Unimed Reusable Finger Clip SpO2 Sensors (U403-49R and U103-49R)Unimed Medical Supplies, Inc.K252448AViTA Pulse Oximeter (SP61)Avita CorporationK252805YUWELL® Finger Pulse Oximeter (YX105, YX106, YX110, YX310)Jiangsu Yuyue Medical Equipment & Supply Co., Ltd.

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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