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FDA 510(k)

KRYSTALONR LIQ. MOUNTING MED.&COVERSLIP

K-Number: K771925 · 1977-11-02

ApplicantHarleco
Decision Date1977-11-02
Product CodeKES
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

KRYSTALONR LIQ. MOUNTING MED.&COVERSLIP is the device name listed in this FDA 510(k) record. The listed applicant is Harleco. It received FDA 510(k) clearance on 1977-11-02 under 510(k) number K771925. The device is classified under product code KES. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 116 devices →

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

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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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