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FDA 510(k)

RPMI-1640 HYBRI-MAX, PROD. NO. R5382

K-Number: K884572 · 1988-11-22

Decision Date1988-11-22
Product CodeKIT
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

RPMI-1640 HYBRI-MAX, PROD. NO. R5382 is the device name listed in this FDA 510(k) record. The listed applicant is Sigma Chemical Co.. It received FDA 510(k) clearance on 1988-11-22 under 510(k) number K884572. 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 HYBRI-MAX, PROD. NO. R5382?

RPMI-1640 HYBRI-MAX, PROD. NO. R5382 is a medical device that received FDA 510(k) clearance on 1988-11-22. The listed applicant is Sigma Chemical Co.. The 510(k) number is K884572.

When did RPMI-1640 HYBRI-MAX, PROD. NO. R5382 receive FDA 510(k) clearance?

RPMI-1640 HYBRI-MAX, PROD. NO. R5382 received FDA 510(k) clearance on 1988-11-22, under 510(k) number K884572.

Who is the listed applicant for RPMI-1640 HYBRI-MAX, PROD. NO. R5382?

The FDA 510(k) record lists Sigma Chemical Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RPMI-1640 HYBRI-MAX, PROD. NO. R5382?

The FDA product code for RPMI-1640 HYBRI-MAX, PROD. NO. R5382 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.

Other records listing Sigma Chemical Co. 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.

View all 231 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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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