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)

HELENA SICKLE-THAL QUIK COLUMN METHOD

K-Number: K812077 · 1981-08-18

ApplicantHelena Laboratories
Decision Date1981-08-18
Product CodeJPD
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

HELENA SICKLE-THAL QUIK COLUMN METHOD is the device name listed in this FDA 510(k) record. The listed applicant is Helena Laboratories. It received FDA 510(k) clearance on 1981-08-18 under 510(k) number K812077. The device is classified under product code JPD. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HELENA SICKLE-THAL QUIK COLUMN METHOD?

HELENA SICKLE-THAL QUIK COLUMN METHOD is a medical device that received FDA 510(k) clearance on 1981-08-18. The listed applicant is Helena Laboratories. The 510(k) number is K812077.

When did HELENA SICKLE-THAL QUIK COLUMN METHOD receive FDA 510(k) clearance?

HELENA SICKLE-THAL QUIK COLUMN METHOD received FDA 510(k) clearance on 1981-08-18, under 510(k) number K812077.

Who is the listed applicant for HELENA SICKLE-THAL QUIK COLUMN METHOD?

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

What is the FDA product code for HELENA SICKLE-THAL QUIK COLUMN METHOD?

The FDA product code for HELENA SICKLE-THAL QUIK COLUMN METHOD is JPD.

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 Helena Laboratories 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.

K131479V8 SP NORMAL CONTROL, ABNORMAL CONTROLK100103SPECIALTY ASSAYED CONTROL-2K061991PLATELETWORKS ARACHIDONIC ACID, MODEL PW-ACAK061069SPIFE IFE-15 PENTAVALENT, MODEL 3456, SPIFE IFE-9 PENTAVALENT KIT, MODEL 3457, SPIFT IFE-6 PENTAVALENT KIT, MODEL 3458K061014ACTALYKE QC KIT, MODELS AQC-HP AND AQC-LPK050053HEMORAM/AGGRAM ANALYZER

View all 280 devices →

Related Devices (Code: JPD)

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.

K020489G7 AUTOMATED HPLC ANALYZER, BETA-THALASSEMIA MODETosoh Medics, Inc.K991127VARIANT II B-THALASSEMIABio-RadK924122VARIANT BETA-THALASSEMIA SHORT PROGRAMBio-RadK924496GLYCOMAT GREEN HBA2 ESTIMATION REAGENT KITDrew Scientific , Ltd.K923318COLUMNMATE BETA-THAL HBA2 CONTROL - NORMALHelena LaboratoriesK923317COLUMNMATE BETA THAL HBA2 CONTROL-ABNORMALHelena Laboratories

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.

↑