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-1640 MEDIUM, CATALOG NO. 210-3525

K-Number: K883630 · 1988-09-07

ApplicantJ R Scientific
Decision Date1988-09-07
Product CodeKIT
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

RPMI-1640 MEDIUM, CATALOG NO. 210-3525 is the device name listed in this FDA 510(k) record. The listed applicant is J R Scientific. It received FDA 510(k) clearance on 1988-09-07 under 510(k) number K883630. 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-1640 MEDIUM, CATALOG NO. 210-3525?

RPMI-1640 MEDIUM, CATALOG NO. 210-3525 is a medical device that received FDA 510(k) clearance on 1988-09-07. The listed applicant is J R Scientific. The 510(k) number is K883630.

When did RPMI-1640 MEDIUM, CATALOG NO. 210-3525 receive FDA 510(k) clearance?

RPMI-1640 MEDIUM, CATALOG NO. 210-3525 received FDA 510(k) clearance on 1988-09-07, under 510(k) number K883630.

Who is the listed applicant for RPMI-1640 MEDIUM, CATALOG NO. 210-3525?

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

What is the FDA product code for RPMI-1640 MEDIUM, CATALOG NO. 210-3525?

The FDA product code for RPMI-1640 MEDIUM, CATALOG NO. 210-3525 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 J R Scientific 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.

K883951MEDIUM 199 W/EBSS (CATALOG NO. 200-2037)K883625EX-CELL 301, CATALOG NO. 200-3651K883631EX-CELL 300TM, CATALOG # 210-3579K883627MIN ESSENT MED EAGLE, JOKLIK MOD, CAT. #200-2150K883628MIN ESSENT MED EAGLE FOR SPINN CULTURE, #200-2051K883632EX-CELL 300TM, CATALOG NO. 210-3575

View all 132 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.

↑