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FDA 510(k)

AUTO. SLIDE STAINER

K-Number: K780017 · 1978-01-30

ApplicantHoneywell, Inc.
Decision Date1978-01-30
Product CodeKPA
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

AUTO. SLIDE STAINER is the device name listed in this FDA 510(k) record. The listed applicant is Honeywell, Inc.. It received FDA 510(k) clearance on 1978-01-30 under 510(k) number K780017. 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 AUTO. SLIDE STAINER?

AUTO. SLIDE STAINER is a medical device that received FDA 510(k) clearance on 1978-01-30. The listed applicant is Honeywell, Inc.. The 510(k) number is K780017.

When did AUTO. SLIDE STAINER receive FDA 510(k) clearance?

AUTO. SLIDE STAINER received FDA 510(k) clearance on 1978-01-30, under 510(k) number K780017.

Who is the listed applicant for AUTO. SLIDE STAINER?

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

What is the FDA product code for AUTO. SLIDE STAINER?

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

Related Clinical Trials

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Other records listing Honeywell, 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.

K902230COLORADO COLOR IMAGING RECORDERK863100CEN STA MON AC/DC ALARM CENTRAL ACCES ALARM RECORK853501HONEYWELL ELECTRONIC VENTILATOR EV-AK855125PHYSIOLOGICAL TELEMETRY PATIENT MONITORING SYSTEMK851888APM DISPOS. BLOOD PRESSURE TRANSDUCERK851496ECG MONITOR MODEL RM102

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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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