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FDA 510(k)

STAIN, R-250, COOMASSIE BRILLIANT BLUE

K-Number: K770718 · 1977-04-26

ApplicantKallestad Laboratories, Inc.
Decision Date1977-04-26
Product CodeJZS
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

STAIN, R-250, COOMASSIE BRILLIANT BLUE is the device name listed in this FDA 510(k) record. The listed applicant is Kallestad Laboratories, Inc.. It received FDA 510(k) clearance on 1977-04-26 under 510(k) number K770718. The device is classified under product code JZS. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STAIN, R-250, COOMASSIE BRILLIANT BLUE?

STAIN, R-250, COOMASSIE BRILLIANT BLUE is a medical device that received FDA 510(k) clearance on 1977-04-26. The listed applicant is Kallestad Laboratories, Inc.. The 510(k) number is K770718.

When did STAIN, R-250, COOMASSIE BRILLIANT BLUE receive FDA 510(k) clearance?

STAIN, R-250, COOMASSIE BRILLIANT BLUE received FDA 510(k) clearance on 1977-04-26, under 510(k) number K770718.

Who is the listed applicant for STAIN, R-250, COOMASSIE BRILLIANT BLUE?

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

What is the FDA product code for STAIN, R-250, COOMASSIE BRILLIANT BLUE?

The FDA product code for STAIN, R-250, COOMASSIE BRILLIANT BLUE is JZS.

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Other records listing Kallestad Laboratories, Inc. as applicant

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Related Devices (Code: JZS)

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.

K933123SYNELISA TG ANTIBODIES/TPO ANTIBODIESElias U.S.A., Inc.K812194IMMUNODIFFUSION BAND INTENSIFYING FLUIDAmerican Scientific ProductsK770566IMMUNOELECTROPHORESIS PROFILE KITKallestad Laboratories, Inc.K770719IMMUNOELECTROFILM KIHKallestad Laboratories, Inc.K770150ELECTRO IMMUNO ASSAY KITMillipore Corp.

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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