KRYSTALONR LIQ. MOUNTING MED.&COVERSLIP
K-Number: K771925 · 1977-11-02
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Device Summary
Frequently Asked Questions
What is the KRYSTALONR LIQ. MOUNTING MED.&COVERSLIP?
KRYSTALONR LIQ. MOUNTING MED.&COVERSLIP is a medical device that received FDA 510(k) clearance on 1977-11-02. The listed applicant is Harleco. The 510(k) number is K771925.
When did KRYSTALONR LIQ. MOUNTING MED.&COVERSLIP receive FDA 510(k) clearance?
KRYSTALONR LIQ. MOUNTING MED.&COVERSLIP received FDA 510(k) clearance on 1977-11-02, under 510(k) number K771925.
Who is the listed applicant for KRYSTALONR LIQ. MOUNTING MED.&COVERSLIP?
The FDA 510(k) record lists Harleco as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KRYSTALONR LIQ. MOUNTING MED.&COVERSLIP?
The FDA product code for KRYSTALONR LIQ. MOUNTING MED.&COVERSLIP is KES.
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 Harleco 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: KES)
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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