MICROSCOPE SLIDES PRECOATED W/HISTOGRIP & POLY-LY
K-Number: K882357 · 1988-06-16
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Device Summary
Frequently Asked Questions
What is the MICROSCOPE SLIDES PRECOATED W/HISTOGRIP & POLY-LY?
MICROSCOPE SLIDES PRECOATED W/HISTOGRIP & POLY-LY is a medical device that received FDA 510(k) clearance on 1988-06-16. The listed applicant is Stat Path. The 510(k) number is K882357.
When did MICROSCOPE SLIDES PRECOATED W/HISTOGRIP & POLY-LY receive FDA 510(k) clearance?
MICROSCOPE SLIDES PRECOATED W/HISTOGRIP & POLY-LY received FDA 510(k) clearance on 1988-06-16, under 510(k) number K882357.
Who is the listed applicant for MICROSCOPE SLIDES PRECOATED W/HISTOGRIP & POLY-LY?
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 W/HISTOGRIP & POLY-LY?
The FDA product code for MICROSCOPE SLIDES PRECOATED W/HISTOGRIP & POLY-LY 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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