Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

RMS 111F RESPIRATORY MONITORING SYSTEM

K-Number: K800086 · 1980-05-08

ApplicantThe Perkin-Elmer Corp.
Decision Date1980-05-08
Product CodeBZK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RMS 111F RESPIRATORY MONITORING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is The Perkin-Elmer Corp.. It received FDA 510(k) clearance on 1980-05-08 under 510(k) number K800086. The device is classified under product code BZK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RMS 111F RESPIRATORY MONITORING SYSTEM?

RMS 111F RESPIRATORY MONITORING SYSTEM is a medical device that received FDA 510(k) clearance on 1980-05-08. The listed applicant is The Perkin-Elmer Corp.. The 510(k) number is K800086.

When did RMS 111F RESPIRATORY MONITORING SYSTEM receive FDA 510(k) clearance?

RMS 111F RESPIRATORY MONITORING SYSTEM received FDA 510(k) clearance on 1980-05-08, under 510(k) number K800086.

Who is the listed applicant for RMS 111F RESPIRATORY MONITORING SYSTEM?

The FDA 510(k) record lists The Perkin-Elmer Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RMS 111F RESPIRATORY MONITORING SYSTEM?

The FDA product code for RMS 111F RESPIRATORY MONITORING SYSTEM is BZK.

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 The Perkin-Elmer Corp. 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.

K935666PERKIN-ELMER SERIES 200 LIQ CHROMATOGRAPHIC PUMPK900828PERKIN-ELMER AA 3100 ATOMIC ABSORPTION SPECTRO.K884864PLASMA 40 INDUCT. COUPLED PLASMA EMMISSION SPECTROK884886MODEL 250 LIQUID CHROMOTAGRAPHY PUMPK872737PERKIN-ELMER LC235 DIODE ARRAY DETECTORK872464ION TRAP DETECTOR (ITD)

View all 62 devices →

Related Devices (Code: BZK)

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.

K260226ElintMAX Respiratory Monitor (ElintMAX Monitor A1)Amptron Medical, Inc.K192584BEACON Caresystem Model 00002144Mermaid Care A/SK192595ExSpiron 2XiRespiratory MotionK180788Gas Module 3Shenzhen Mindray Bio-Medical Electronics Co., Ltd.K173181ExSpiron 1XiRespiratory Motion, Inc.K162131ExSpiron 1XiRespiratory Motion, Inc.

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.

↑