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FDA 510(k)

SLIDE STAINERS GLS 360 & 360-1

K-Number: K771714 · 1977-10-05

ApplicantHoneywell, Inc.
Decision Date1977-10-05
Product CodeKEY
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

SLIDE STAINERS GLS 360 & 360-1 is the device name listed in this FDA 510(k) record. The listed applicant is Honeywell, Inc.. It received FDA 510(k) clearance on 1977-10-05 under 510(k) number K771714. The device is classified under product code KEY. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SLIDE STAINERS GLS 360 & 360-1?

SLIDE STAINERS GLS 360 & 360-1 is a medical device that received FDA 510(k) clearance on 1977-10-05. The listed applicant is Honeywell, Inc.. The 510(k) number is K771714.

When did SLIDE STAINERS GLS 360 & 360-1 receive FDA 510(k) clearance?

SLIDE STAINERS GLS 360 & 360-1 received FDA 510(k) clearance on 1977-10-05, under 510(k) number K771714.

Who is the listed applicant for SLIDE STAINERS GLS 360 & 360-1?

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 SLIDE STAINERS GLS 360 & 360-1?

The FDA product code for SLIDE STAINERS GLS 360 & 360-1 is KEY.

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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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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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