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FDA 510(k)

STAIN KIT FOR CELL CULTURES (30-100-00)

K-Number: K781875 · 1978-12-20

ApplicantFlow Laboratories, Inc.
Decision Date1978-12-20
Product CodeKPB
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

STAIN KIT FOR CELL CULTURES (30-100-00) is the device name listed in this FDA 510(k) record. The listed applicant is Flow Laboratories, Inc.. It received FDA 510(k) clearance on 1978-12-20 under 510(k) number K781875. The device is classified under product code KPB. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STAIN KIT FOR CELL CULTURES (30-100-00)?

STAIN KIT FOR CELL CULTURES (30-100-00) is a medical device that received FDA 510(k) clearance on 1978-12-20. The listed applicant is Flow Laboratories, Inc.. The 510(k) number is K781875.

When did STAIN KIT FOR CELL CULTURES (30-100-00) receive FDA 510(k) clearance?

STAIN KIT FOR CELL CULTURES (30-100-00) received FDA 510(k) clearance on 1978-12-20, under 510(k) number K781875.

Who is the listed applicant for STAIN KIT FOR CELL CULTURES (30-100-00)?

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

What is the FDA product code for STAIN KIT FOR CELL CULTURES (30-100-00)?

The FDA product code for STAIN KIT FOR CELL CULTURES (30-100-00) is KPB.

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Other records listing Flow 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.

K861897UNISKAN IIK862066TITERTEK MICROPLATE WASHER S-12K861791PENICILLIN-STREPTOMYCIN-FUNGIZONEK861824GENTAMICIN SULFATE SOLUTION (10MG GENTAMICIN)K861823GENTAMICIN SULFATE SOLUTION (50MG GENTAMICIN)K860762GAMMA-FREE HORSE SERUM

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Related Devices (Code: KPB)

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.

K781874MYCOPLASMA ARGININI FITC (30-403-41)Flow Laboratories, Inc.K781390MYCOPLASMA HYORHINIS (BTS-7)Flow Laboratories, Inc.K771867MYCOPLASMA DETECTION KITBioassay Systems Research 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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