MICRO THIN* PARAFFIN
K-Number: K862223 · 1986-06-17
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Device Summary
Frequently Asked Questions
What is the MICRO THIN* PARAFFIN?
MICRO THIN* PARAFFIN is a medical device that received FDA 510(k) clearance on 1986-06-17. The listed applicant is Richard-Allan Medical Ind., Inc.. The 510(k) number is K862223.
When did MICRO THIN* PARAFFIN receive FDA 510(k) clearance?
MICRO THIN* PARAFFIN received FDA 510(k) clearance on 1986-06-17, under 510(k) number K862223.
Who is the listed applicant for MICRO THIN* PARAFFIN?
The FDA 510(k) record lists Richard-Allan Medical Ind., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MICRO THIN* PARAFFIN?
The FDA product code for MICRO THIN* PARAFFIN is KEO.
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 Richard-Allan Medical Ind., Inc. 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: KEO)
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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