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)

LIQUID SCINTILLATION COUNTER

K-Number: K780179 · 1978-02-23

ApplicantRoche Medical Electronics, Inc.
Decision Date1978-02-23
Product CodeJJJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LIQUID SCINTILLATION COUNTER is the device name listed in this FDA 510(k) record. The listed applicant is Roche Medical Electronics, Inc.. It received FDA 510(k) clearance on 1978-02-23 under 510(k) number K780179. The device is classified under product code JJJ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIQUID SCINTILLATION COUNTER?

LIQUID SCINTILLATION COUNTER is a medical device that received FDA 510(k) clearance on 1978-02-23. The listed applicant is Roche Medical Electronics, Inc.. The 510(k) number is K780179.

When did LIQUID SCINTILLATION COUNTER receive FDA 510(k) clearance?

LIQUID SCINTILLATION COUNTER received FDA 510(k) clearance on 1978-02-23, under 510(k) number K780179.

Who is the listed applicant for LIQUID SCINTILLATION COUNTER?

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

What is the FDA product code for LIQUID SCINTILLATION COUNTER?

The FDA product code for LIQUID SCINTILLATION COUNTER is JJJ.

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 Roche Medical Electronics, 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.

K791559ROCHE SENSOR ADAPTORK791038FETASONDE UTERINE ACTIVITY MONITORK791039FETASONDE FETAL HEART RATE VARIABILITYK791035FETASONDE FETAL ACTIVITY MONITORK791037FETASONDE LABOR STATUS DISPLAYK791036FETASONDE UTERINE WORK MONITOR

View all 16 devices →

Related Devices (Code: JJJ)

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.

K962762SEQUENTIAL SAMPLE MULTI-PHOTON DETECTORBiotraces, Inc.K946387CAPRA (CAPRAC-R) WIPETEST AND WELL COUNTERCapintec, Inc.K920559ABBOTT VERTEX ANALYZERAbbott LaboratoriesK900087GENESYS 6000 GAMMA COUNTERLaboratory Technologies, Inc.K896202MATRIX(TM)-96Canberra Industries, Inc.K894902SOURCEREROakfield Instruments, Ltd.

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.

↑