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FDA 510(k)

LX-100 SLIDE STAINER

K-Number: K880745 · 1988-04-27

ApplicantInnovative Medical Systems, Inc.
Decision Date1988-04-27
Product CodeKPA
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

LX-100 SLIDE STAINER is the device name listed in this FDA 510(k) record. The listed applicant is Innovative Medical Systems, Inc.. It received FDA 510(k) clearance on 1988-04-27 under 510(k) number K880745. 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 LX-100 SLIDE STAINER?

LX-100 SLIDE STAINER is a medical device that received FDA 510(k) clearance on 1988-04-27. The listed applicant is Innovative Medical Systems, Inc.. The 510(k) number is K880745.

When did LX-100 SLIDE STAINER receive FDA 510(k) clearance?

LX-100 SLIDE STAINER received FDA 510(k) clearance on 1988-04-27, under 510(k) number K880745.

Who is the listed applicant for LX-100 SLIDE STAINER?

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

What is the FDA product code for LX-100 SLIDE STAINER?

The FDA product code for LX-100 SLIDE STAINER is KPA. This falls under the Cardiovascular category.

Related Clinical Trials

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.

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Other records listing Innovative Medical Systems, 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.

K973035VIOLA II DENTAL CAMERA SYSTEMK951469BAZOOKA SYSTEMK933184POSITIVE AIRWAY PRESSURE SYSTEMK924590MICROWAVE AUTOMATED TISSUE PROCESSORK922081LABOTECH AUTOMATED MICROTITER ANALYZERK921005AUTOLOADER

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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.K874887WESBLOT PROCESSORAmerican Bionetics, Inc.K874897SAKURA DRS-60 AUTOMATIC SLIDE STAINERSakura Finetek U.S.A., Inc.K872916HISTOMATIC SLIDE STAINER, CODE-ON VERSIONFisher Scientific Co., LLC

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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