Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MICRO THIN* PARAFFIN

K-Number: K862223 · 1986-06-17

Decision Date1986-06-17
Product CodeKEO
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

MICRO THIN* PARAFFIN is the device name listed in this FDA 510(k) record. The listed applicant is Richard-Allan Medical Ind., Inc.. It received FDA 510(k) clearance on 1986-06-17 under 510(k) number K862223. The device is classified under product code KEO. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 33 devices →

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.

↑