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FDA 510(k)

S-MEM-JOKLIK'S POWDER

K-Number: K821911 · 1982-07-27

ApplicantDutchland Laboratories, Inc.
Decision Date1982-07-27
Product CodeKIT
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

S-MEM-JOKLIK'S POWDER is the device name listed in this FDA 510(k) record. The listed applicant is Dutchland Laboratories, Inc.. It received FDA 510(k) clearance on 1982-07-27 under 510(k) number K821911. 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 S-MEM-JOKLIK'S POWDER?

S-MEM-JOKLIK'S POWDER is a medical device that received FDA 510(k) clearance on 1982-07-27. The listed applicant is Dutchland Laboratories, Inc.. The 510(k) number is K821911.

When did S-MEM-JOKLIK'S POWDER receive FDA 510(k) clearance?

S-MEM-JOKLIK'S POWDER received FDA 510(k) clearance on 1982-07-27, under 510(k) number K821911.

Who is the listed applicant for S-MEM-JOKLIK'S POWDER?

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

What is the FDA product code for S-MEM-JOKLIK'S POWDER?

The FDA product code for S-MEM-JOKLIK'S POWDER is KIT.

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Other records listing Dutchland Laboratories, 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.

K821912MCCOY'S POWDER MEDIUM 5A SUSPENSIONK821918POWDERED RPMI-1603 MEDIUMK821916IMPROVED MEM-RICHTER'S POWDER MODIF.K821917WAYMOUTH'S POWDER MEDIUMK821915BME AUTOCLAVABLE MEDIUMK821913ISCOVE'S MODIFIED DULBECCO POWDER MEDIUM

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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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