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)

ULTRASONIC FLOWMETER

K-Number: K800087 · 1980-03-19

ApplicantThe Perkin-Elmer Corp.
Decision Date1980-03-19
Product CodeBXP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ULTRASONIC FLOWMETER 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 1980-03-19 under 510(k) number K800087. The device is classified under product code BXP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTRASONIC FLOWMETER?

ULTRASONIC FLOWMETER is a medical device that received FDA 510(k) clearance on 1980-03-19. The listed applicant is The Perkin-Elmer Corp.. The 510(k) number is K800087.

When did ULTRASONIC FLOWMETER receive FDA 510(k) clearance?

ULTRASONIC FLOWMETER received FDA 510(k) clearance on 1980-03-19, under 510(k) number K800087.

Who is the listed applicant for ULTRASONIC FLOWMETER?

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 ULTRASONIC FLOWMETER?

The FDA product code for ULTRASONIC FLOWMETER is BXP.

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: BXP)

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.

K936141UNIPOWER RECHARGEABLE BATTERY PACKUnipower Corp.K920360TIMOX OXYGEN TIMERMedical Fittings, Inc.K832678PHONATORY FUNCTION ANALYZER PS-77Kells Medical, Inc.K781039OXY-ON DIGITAL OXYGEN TIMERChambers & Sadler Mfg.K770424OXYGEN TWMER, MODEL SSTTimeter Instrument Corp.K761260ARIZONA OXYGEN TIMER DEVICEThe John Bunn Co.

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.

↑