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)

QUICK PRIME HEMOCONCEN. NO. HQ-7000 AND CBP-7000Q

K-Number: K903641 · 1990-11-09

ApplicantBentley Laboratories, Inc.
Decision Date1990-11-09
Product CodeKDI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

QUICK PRIME HEMOCONCEN. NO. HQ-7000 AND CBP-7000Q is the device name listed in this FDA 510(k) record. The listed applicant is Bentley Laboratories, Inc.. It received FDA 510(k) clearance on 1990-11-09 under 510(k) number K903641. The device is classified under product code KDI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUICK PRIME HEMOCONCEN. NO. HQ-7000 AND CBP-7000Q?

QUICK PRIME HEMOCONCEN. NO. HQ-7000 AND CBP-7000Q is a medical device that received FDA 510(k) clearance on 1990-11-09. The listed applicant is Bentley Laboratories, Inc.. The 510(k) number is K903641.

When did QUICK PRIME HEMOCONCEN. NO. HQ-7000 AND CBP-7000Q receive FDA 510(k) clearance?

QUICK PRIME HEMOCONCEN. NO. HQ-7000 AND CBP-7000Q received FDA 510(k) clearance on 1990-11-09, under 510(k) number K903641.

Who is the listed applicant for QUICK PRIME HEMOCONCEN. NO. HQ-7000 AND CBP-7000Q?

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

What is the FDA product code for QUICK PRIME HEMOCONCEN. NO. HQ-7000 AND CBP-7000Q?

The FDA product code for QUICK PRIME HEMOCONCEN. NO. HQ-7000 AND CBP-7000Q is KDI.

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 Bentley Laboratories, 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.

K931967HE-30 GOLDK913956BLOOD CARDIOPLEGIA HEAT EXCHANGER, MODEL #HE-30K913692VENOUS RESERVOIR BAG MODEL NO. BMR-250(TM)K894826UNIVOX W/HOLDERS, MODELS UNIVOX-HL, HLB, HLFK874867CATR(TM)-H CARDIOTOMY HOLDERK874841INTEGRATED MEMBRANE OXYGENATOR W/CARDIOTOMY FILTER

View all 55 devices →

Related Devices (Code: KDI)

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.

K261267Careflux H60;Careflux H70;Careflux V500Fresenius Medical Care Renal Therapies Group, LLCK252377NxStage System One with NxViewFresenius Medical Care Renal Therapies Group, LLCK260533ELISIO™-HNipro Medical CorporationK252459multiFlux 130 (F00013123); multiFlux 160 (F00013124)Fresenius Medical Care Renal Therapies Group, LLCK253412Tablo Hemodialysis System (PN-0008000, PN-0006000U)Outset Medical, Inc.K253518FX CorAL 40; FX CorAL 50Fresenius Medical Care Renal Therapies Group, LLC

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.

↑