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)

CESIUM DILUENT 1.5 MMOL CS/L #60087

K-Number: K871186 · 1987-05-28

ApplicantIn Vitro Diagnostics, Inc.
Decision Date1987-05-28
Product CodeJIS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CESIUM DILUENT 1.5 MMOL CS/L #60087 is the device name listed in this FDA 510(k) record. The listed applicant is In Vitro Diagnostics, Inc.. It received FDA 510(k) clearance on 1987-05-28 under 510(k) number K871186. The device is classified under product code JIS. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CESIUM DILUENT 1.5 MMOL CS/L #60087?

CESIUM DILUENT 1.5 MMOL CS/L #60087 is a medical device that received FDA 510(k) clearance on 1987-05-28. The listed applicant is In Vitro Diagnostics, Inc.. The 510(k) number is K871186.

When did CESIUM DILUENT 1.5 MMOL CS/L #60087 receive FDA 510(k) clearance?

CESIUM DILUENT 1.5 MMOL CS/L #60087 received FDA 510(k) clearance on 1987-05-28, under 510(k) number K871186.

Who is the listed applicant for CESIUM DILUENT 1.5 MMOL CS/L #60087?

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

What is the FDA product code for CESIUM DILUENT 1.5 MMOL CS/L #60087?

The FDA product code for CESIUM DILUENT 1.5 MMOL CS/L #60087 is JIS.

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 In Vitro Diagnostics, 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.

K896867THYROID STIMULATING HORMONE-EIA-XTK896863DIGOXIN-EIA-XTK896866LUTEINIZING HORMONE-EIA-XTK896865VITRO T4-EIA-XTK896925T UPTAKE ENZYME IMMUNOASSAY CRIMPED TUBE KITK896864FOLLICLE STIMULATING HORMONE-EIA-XT

View all 15 devices →

Related Devices (Code: JIS)

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.

K122126DIRECT LDL/HDL CHOLESTEROL CALIBRATORRandox Laboratories LimitedK061251DIMENSION VISTA TOTAL IRON BINDING CAPACITY CALIBRATORDade Behring, Inc.K060266DIMENSION IRON CALIBRATORDade Behring, Inc.K053104DIMENSION CARDIOPHASE HIGH SENSITIVITY C-REACTIVE PROTEIN CALIBRATORDade Behring, Inc.K032697DIMENSION TOTAL TRIIODOTHYRONINE CALIBRATOR (RC414)Dade Behring, Inc.K032608GONOTEC CALIBRATION SOLUTION 300 MOSMOL/KG FOR OSMOMETERGonotec Gesellschaft Fuer Mess-Und Regeltechnik MB

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.

↑