CHROLOY SOLDER
K-Number: K021965 · 2002-07-26
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Device Summary
Frequently Asked Questions
What is the CHROLOY SOLDER?
CHROLOY SOLDER is a medical device that received FDA 510(k) clearance on 2002-07-26. The listed applicant is Neirynck & Vogt NV. The 510(k) number is K021965.
When did CHROLOY SOLDER receive FDA 510(k) clearance?
CHROLOY SOLDER received FDA 510(k) clearance on 2002-07-26, under 510(k) number K021965.
Who is the listed applicant for CHROLOY SOLDER?
The FDA 510(k) record lists Neirynck & Vogt NV as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CHROLOY SOLDER?
The FDA product code for CHROLOY SOLDER is EJH.
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 Neirynck & Vogt NV 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: EJH)
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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