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)

RPMI-1634 MEDIUM

K-Number: K850230 · 1985-03-05

ApplicantHazleton Research Products, Inc.
Decision Date1985-03-05
Product CodeKIT
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

RPMI-1634 MEDIUM is the device name listed in this FDA 510(k) record. The listed applicant is Hazleton Research Products, Inc.. It received FDA 510(k) clearance on 1985-03-05 under 510(k) number K850230. The device is classified under product code KIT. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RPMI-1634 MEDIUM?

RPMI-1634 MEDIUM is a medical device that received FDA 510(k) clearance on 1985-03-05. The listed applicant is Hazleton Research Products, Inc.. The 510(k) number is K850230.

When did RPMI-1634 MEDIUM receive FDA 510(k) clearance?

RPMI-1634 MEDIUM received FDA 510(k) clearance on 1985-03-05, under 510(k) number K850230.

Who is the listed applicant for RPMI-1634 MEDIUM?

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

What is the FDA product code for RPMI-1634 MEDIUM?

The FDA product code for RPMI-1634 MEDIUM is KIT.

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 Hazleton Research Products, 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.

K861997PENICILLIN-STREPTOMYCIN-FUNGIZONE MIXTUREK861996DULBECCO'S MEM WITH 4.5 G/L GLUCOSE MEDIUMK861886DMEM & HAM'S F-12 (1:1) POWDERED MEDIUMK861869GENTAMICIN-50MG/MLK861872ISCOVE'S (MODIFIED) DULBECCO'S MEDIUMK861871NCTC 109 MEDIUM

View all 47 devices →

Related Devices (Code: KIT)

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.

K892938AMNIO-GROW TMInovar Biologicals, Inc.K890700MELANOCYTE GROWTH MEDIUM (MGM)Clonetics Corp.K890701ENDOTHELIAL GROWTH MEDIUM (EGM)Clonetics Corp.K890482ABC, ABC-1X, ABC(TM)Cell Ent., Inc.K884654ALPHACALF SERUMHyclone Laboratories, Inc.K884572RPMI-1640 HYBRI-MAX, PROD. NO. R5382Sigma Chemical Co.

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.

↑