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FDA 510(k)

QUIK-STAIN

K-Number: K790571 · 1979-04-23

ApplicantDade, Baxter Travenol Diagnostics, Inc.
Decision Date1979-04-23
Product CodeIAF
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

QUIK-STAIN is the device name listed in this FDA 510(k) record. The listed applicant is Dade, Baxter Travenol Diagnostics, Inc.. It received FDA 510(k) clearance on 1979-04-23 under 510(k) number K790571. The device is classified under product code IAF. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUIK-STAIN?

QUIK-STAIN is a medical device that received FDA 510(k) clearance on 1979-04-23. The listed applicant is Dade, Baxter Travenol Diagnostics, Inc.. The 510(k) number is K790571.

When did QUIK-STAIN receive FDA 510(k) clearance?

QUIK-STAIN received FDA 510(k) clearance on 1979-04-23, under 510(k) number K790571.

Who is the listed applicant for QUIK-STAIN?

The FDA 510(k) record lists Dade, Baxter Travenol Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for QUIK-STAIN?

The FDA product code for QUIK-STAIN is IAF.

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Other records listing Dade, Baxter Travenol Diagnostics, Inc. as applicant

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Related Devices (Code: IAF)

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K890673WRIGHT-GLEMSA STAINSigma Diagnostics, Inc.K890674ACCUSTAIN(TM) - AUTOMATED WRIGHT GIEMSA STAIN SETSigma Diagnostics, Inc.K854236HISTAMINE RIA TEST FOR HISTAMINE BIOLOGICAL FLUIDSNms Pharmaceuticals, Inc.K860793CAMCO STAIN PAKCambridge Chemical Products, Inc.K853241HEMATOLOGY STAIN PACKFisher Scientific Co., LLCK852138WESCOR STAIN PACK FOR MODEL 7100 AEROSPRAY SLIDE SCanyon Diagnostics, Inc.

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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