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FDA 510(k)

ISCOVE'S MODIFIED DULBECCO'S MEDIUM (IMDM)

K-Number: K873022 · 1987-08-19

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

Device Summary

ISCOVE'S MODIFIED DULBECCO'S MEDIUM (IMDM) 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 K873022. 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 ISCOVE'S MODIFIED DULBECCO'S MEDIUM (IMDM)?

ISCOVE'S MODIFIED DULBECCO'S MEDIUM (IMDM) 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 K873022.

When did ISCOVE'S MODIFIED DULBECCO'S MEDIUM (IMDM) receive FDA 510(k) clearance?

ISCOVE'S MODIFIED DULBECCO'S MEDIUM (IMDM) received FDA 510(k) clearance on 1987-08-19, under 510(k) number K873022.

Who is the listed applicant for ISCOVE'S MODIFIED DULBECCO'S MEDIUM (IMDM)?

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 ISCOVE'S MODIFIED DULBECCO'S MEDIUM (IMDM)?

The FDA product code for ISCOVE'S MODIFIED DULBECCO'S MEDIUM (IMDM) 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

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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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