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)

PRESERV CARY BLAIR TRANSPORT PACK

K-Number: K840990 · 1984-03-23

ApplicantPreventive Diagnostics Corp.
Decision Date1984-03-23
Product CodeJTW
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

PRESERV CARY BLAIR TRANSPORT PACK is the device name listed in this FDA 510(k) record. The listed applicant is Preventive Diagnostics Corp.. It received FDA 510(k) clearance on 1984-03-23 under 510(k) number K840990. The device is classified under product code JTW. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRESERV CARY BLAIR TRANSPORT PACK?

PRESERV CARY BLAIR TRANSPORT PACK is a medical device that received FDA 510(k) clearance on 1984-03-23. The listed applicant is Preventive Diagnostics Corp.. The 510(k) number is K840990.

When did PRESERV CARY BLAIR TRANSPORT PACK receive FDA 510(k) clearance?

PRESERV CARY BLAIR TRANSPORT PACK received FDA 510(k) clearance on 1984-03-23, under 510(k) number K840990.

Who is the listed applicant for PRESERV CARY BLAIR TRANSPORT PACK?

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

What is the FDA product code for PRESERV CARY BLAIR TRANSPORT PACK?

The FDA product code for PRESERV CARY BLAIR TRANSPORT PACK is JTW.

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 Preventive Diagnostics 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.

K840677HDL EZ-TZ3 CHOLESTEROL REAGENT KITK840676PDC HDL EZ-SEP CHOLESTEROL REAGENTK840219TRIGLYCERIDE/CHOLESTEROL AQUEOUSK840220HDL CHOLESTEROL AQUEOUS STANDARDSK840278HDL CHOLESTEROL CONTROLS-LEVELSK840968PRESERV TRANSPORT & CULTURE PACK

View all 18 devices →

Related Devices (Code: JTW)

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.

K121039COPAN MSWAB COLLECTION, TRANSPORT AND PRESERVATION SYSTEMCopan Flock TechnologiesK061301COPAN LIQUID AMIES ELUTION SWAB (ESWAB) COLLECTION AND TRANSPORT SYSTEMCopan Diagnostics, Inc.K022874GEN-PROBE APTIMA COMBO 2 ASSAYGen-Probe, Inc.K013819URINE COLLECTION, PRESERVATION AND TRANSPORT SYSTEMSierra Diagnostic, LLCK993161COPAN EASY-SWAB COLLECTION AND TRANSPORT SYSTEMCopan Diagnostics, Inc.K983244SENSITITRE 18-24 HR SUSCEPTIBILITY PLATES(ADDITION OF MEROPENEM)Trek Diagnostic Systems, 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.

↑