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)

ORX DENT-AIDE DENTAL EMERGENCY KIT

K-Number: K820501 · 1982-04-19

Decision Date1982-04-19
Product Code
DecisionSubstantially Equivalent

Device Summary

ORX DENT-AIDE DENTAL EMERGENCY KIT is the device name listed in this FDA 510(k) record. The listed applicant is Dental Aide Products. It received FDA 510(k) clearance on 1982-04-19 under 510(k) number K820501. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ORX DENT-AIDE DENTAL EMERGENCY KIT?

ORX DENT-AIDE DENTAL EMERGENCY KIT is a medical device that received FDA 510(k) clearance on 1982-04-19. The listed applicant is Dental Aide Products. The 510(k) number is K820501.

When did ORX DENT-AIDE DENTAL EMERGENCY KIT receive FDA 510(k) clearance?

ORX DENT-AIDE DENTAL EMERGENCY KIT received FDA 510(k) clearance on 1982-04-19, under 510(k) number K820501.

Who is the listed applicant for ORX DENT-AIDE DENTAL EMERGENCY KIT?

The FDA 510(k) record lists Dental Aide Products as the applicant. This does not by itself establish the device manufacturer.

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.

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.

↑