MICROSCOPE SLIDES PRECOATED
K-Number: K890042 · 1989-01-13
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Device Summary
Frequently Asked Questions
What is the MICROSCOPE SLIDES PRECOATED?
MICROSCOPE SLIDES PRECOATED is a medical device that received FDA 510(k) clearance on 1989-01-13. The listed applicant is Stat Path. The 510(k) number is K890042.
When did MICROSCOPE SLIDES PRECOATED receive FDA 510(k) clearance?
MICROSCOPE SLIDES PRECOATED received FDA 510(k) clearance on 1989-01-13, under 510(k) number K890042.
Who is the listed applicant for MICROSCOPE SLIDES PRECOATED?
The FDA 510(k) record lists Stat Path as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MICROSCOPE SLIDES PRECOATED?
The FDA product code for MICROSCOPE SLIDES PRECOATED is KEW.
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.
Other records listing Stat Path 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.
Related Devices (Code: KEW)
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.
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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