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)

S/P VORTEX MIXER

K-Number: K813148 · 1981-11-24

ApplicantAmerican Dade
Decision Date1981-11-24
Product CodeJRQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

S/P VORTEX MIXER is the device name listed in this FDA 510(k) record. The listed applicant is American Dade. It received FDA 510(k) clearance on 1981-11-24 under 510(k) number K813148. The device is classified under product code JRQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the S/P VORTEX MIXER?

S/P VORTEX MIXER is a medical device that received FDA 510(k) clearance on 1981-11-24. The listed applicant is American Dade. The 510(k) number is K813148.

When did S/P VORTEX MIXER receive FDA 510(k) clearance?

S/P VORTEX MIXER received FDA 510(k) clearance on 1981-11-24, under 510(k) number K813148.

Who is the listed applicant for S/P VORTEX MIXER?

The FDA 510(k) record lists American Dade as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for S/P VORTEX MIXER?

The FDA product code for S/P VORTEX MIXER is JRQ.

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 American Dade 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.

K873051STRATUS(R) HFSH FLUOROMETRIC ENZYME IMMUNOASSAYK873171STRATUS(R) CK-MB FLUOROMETRIC ENZYME IMMUNOASSAYK873052STRATUS(R) HLH FLUOROMETRIC ENZYME IMMUNOASSAYK872789PARAMAX URINE/CSF CALIBRATORK872195DATA-FI DIMERTEST LATEX ASSAYK872196AQUEOUS BLOOD GAS/ELECTROLYTE CONTR LEV I,II & III

View all 149 devices →

Related Devices (Code: JRQ)

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.

K813318MINI-SHAKERDynatech Corp.K813149S/P VORTEX MIXER JR.American DadeK801145SMI MULTI-TUBE VORTEXERScientific Manufacturing IndustriesK790753DIMENSIONALL ROTATORAmerican Hospital Supply Corp.K790027SHAKER, MODEL SH-510Sysmex Corp.K780543THERMAJUST CIRCU-TEMPTechhnilab Instruments, 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.

↑