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)

COMFORT CUSHION DISPOS. ANALGESIS

K-Number: K832752 · 1983-12-08

Decision Date1983-12-08
Product CodeCBN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

COMFORT CUSHION DISPOS. ANALGESIS is the device name listed in this FDA 510(k) record. The listed applicant is Mission Dental, Inc.. It received FDA 510(k) clearance on 1983-12-08 under 510(k) number K832752. The device is classified under product code CBN. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMFORT CUSHION DISPOS. ANALGESIS?

COMFORT CUSHION DISPOS. ANALGESIS is a medical device that received FDA 510(k) clearance on 1983-12-08. The listed applicant is Mission Dental, Inc.. The 510(k) number is K832752.

When did COMFORT CUSHION DISPOS. ANALGESIS receive FDA 510(k) clearance?

COMFORT CUSHION DISPOS. ANALGESIS received FDA 510(k) clearance on 1983-12-08, under 510(k) number K832752.

Who is the listed applicant for COMFORT CUSHION DISPOS. ANALGESIS?

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

What is the FDA product code for COMFORT CUSHION DISPOS. ANALGESIS?

The FDA product code for COMFORT CUSHION DISPOS. ANALGESIS is CBN.

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 Mission Dental, 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: CBN)

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.

↑