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FDA 510(k)

RPMI-1640 W/L-GLUTAMINE AND W/O SODIUM BICARBONATE

K-Number: K873023 · 1987-08-19

ApplicantJ R Scientific
Decision Date1987-08-19
Product CodeKIT
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

RPMI-1640 W/L-GLUTAMINE AND W/O SODIUM BICARBONATE 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 1987-08-19 under 510(k) number K873023. 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 W/L-GLUTAMINE AND W/O SODIUM BICARBONATE?

RPMI-1640 W/L-GLUTAMINE AND W/O SODIUM BICARBONATE is a medical device that received FDA 510(k) clearance on 1987-08-19. The listed applicant is J R Scientific. The 510(k) number is K873023.

When did RPMI-1640 W/L-GLUTAMINE AND W/O SODIUM BICARBONATE receive FDA 510(k) clearance?

RPMI-1640 W/L-GLUTAMINE AND W/O SODIUM BICARBONATE received FDA 510(k) clearance on 1987-08-19, under 510(k) number K873023.

Who is the listed applicant for RPMI-1640 W/L-GLUTAMINE AND W/O SODIUM BICARBONATE?

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 W/L-GLUTAMINE AND W/O SODIUM BICARBONATE?

The FDA product code for RPMI-1640 W/L-GLUTAMINE AND W/O SODIUM BICARBONATE is KIT.

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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.

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