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FDA 510(k)

HISTOMATIC SLIDE STAINER, CODE-ON VERSION

K-Number: K872916 · 1987-09-14

ApplicantFisher Scientific Co., LLC
Decision Date1987-09-14
Product CodeKPA
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

HISTOMATIC SLIDE STAINER, CODE-ON VERSION is the device name listed in this FDA 510(k) record. The listed applicant is Fisher Scientific Co., LLC. It received FDA 510(k) clearance on 1987-09-14 under 510(k) number K872916. The device is classified under product code KPA. It was reviewed by the PA advisory panel. Product code KPA falls under the category of Cardiovascular, which encompasses devices for cardiovascular diagnosis, monitoring, and intervention. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HISTOMATIC SLIDE STAINER, CODE-ON VERSION?

HISTOMATIC SLIDE STAINER, CODE-ON VERSION is a medical device that received FDA 510(k) clearance on 1987-09-14. The listed applicant is Fisher Scientific Co., LLC. The 510(k) number is K872916.

When did HISTOMATIC SLIDE STAINER, CODE-ON VERSION receive FDA 510(k) clearance?

HISTOMATIC SLIDE STAINER, CODE-ON VERSION received FDA 510(k) clearance on 1987-09-14, under 510(k) number K872916.

Who is the listed applicant for HISTOMATIC SLIDE STAINER, CODE-ON VERSION?

The FDA 510(k) record lists Fisher Scientific Co., LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HISTOMATIC SLIDE STAINER, CODE-ON VERSION?

The FDA product code for HISTOMATIC SLIDE STAINER, CODE-ON VERSION is KPA. This falls under the Cardiovascular category.

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Other records listing Fisher Scientific Co., LLC 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.

K930415MICROHEMATOCRIT ROTORK915825MARATHON 6K GENERAL-PURPOSE CENTRIFUGEK915441MARATHON 13K/H MICROHEMATOCRIT CENTRIFUGEK890534MODIFIED URIQUAL(TM) URINALYSIS CONTROL LEVEL 1K881275URIQUAL(TM) URINALYSIS CONTROLS (HUMAN) I & IIK874054FISHER DIAGNOSTICS HEMATALL III LAS REAGENT

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Related Devices (Code: KPA)

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.

K933996PROFIBLOTTecan U.S., Ltd.K884258VERSABLOTAmerican Bionetics, Inc.K881592WESCOR MODEL 7300 AEROSPRAY GRAM STAINERWescor, Inc.K880745LX-100 SLIDE STAINERInnovative Medical Systems, Inc.K874887WESBLOT PROCESSORAmerican Bionetics, Inc.K874897SAKURA DRS-60 AUTOMATIC SLIDE STAINERSakura Finetek U.S.A., 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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