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)

DENTAL NEEDLE (CARTRIDGE TYPE)

K-Number: K870921 · 1987-04-03

Decision Date1987-04-03
Product CodeDZM
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DENTAL NEEDLE (CARTRIDGE TYPE) is the device name listed in this FDA 510(k) record. The listed applicant is Churchill Corp.. It received FDA 510(k) clearance on 1987-04-03 under 510(k) number K870921. The device is classified under product code DZM. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DENTAL NEEDLE (CARTRIDGE TYPE)?

DENTAL NEEDLE (CARTRIDGE TYPE) is a medical device that received FDA 510(k) clearance on 1987-04-03. The listed applicant is Churchill Corp.. The 510(k) number is K870921.

When did DENTAL NEEDLE (CARTRIDGE TYPE) receive FDA 510(k) clearance?

DENTAL NEEDLE (CARTRIDGE TYPE) received FDA 510(k) clearance on 1987-04-03, under 510(k) number K870921.

Who is the listed applicant for DENTAL NEEDLE (CARTRIDGE TYPE)?

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

What is the FDA product code for DENTAL NEEDLE (CARTRIDGE TYPE)?

The FDA product code for DENTAL NEEDLE (CARTRIDGE TYPE) is DZM.

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 Churchill Corp. 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 35 devices →

Related Devices (Code: DZM)

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.

↑