DENTAL NEEDLE (CARTRIDGE TYPE)— 510(k) K870921

Name: FDA 510(k) clearance K870921
Creator: U.S. Food and Drug Administration
Published: 1987-04-03

Substantially Equivalent

Churchill Corp.

FDA 510(k) clearance K870921 for DENTAL NEEDLE (CARTRIDGE TYPE), Substantially Equivalent on 1987-04-03. Applicant: Churchill Corp.. Device class: 1.

Clearance details

Applicant: Churchill Corp.
Product code: Code DZM
Device class: Class 1
Regulation: 21 CFR 872.4730
Advisory panel: Dental
Date received: 1987-03-05
Decision date: 1987-04-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Langhorne, PA, US

Download summary PDF View on FDA.gov ↗

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K990511 — X-TIP INTRAOSSEOUS PERFORATOR1999-04-27
K920758 — JENKER NEEDLE STICK PROTECTOR1992-04-28
K914562 — ASEPTIC DENTAL TECH. TOTAL TREATMENT SYSTEM1992-03-09
K913573 — SAFETY PLUS DENTAL INJECTION NEEDLE1991-11-07
K910475 — DENTAL NEEDLE PROTECTIVE SYSTEM1991-09-13

More clearances from Churchill Corp.

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K880025 — CHURCHILL 0.22 MICRON LIQUID FILTER SETS1988-04-14
K880026 — CHURCHILL 0.22 MICRON LIQUID COMPACT FILTER SETS1988-04-14
K880051 — ENTERAL BAG/SET1988-04-14
K880027 — CHURCHILL 1.2 MICRON LIQUID FILTER SET1988-04-13
K870395 — CHURCHILL PARENTERAL NUTRITION BAG - EVA1987-10-15

Adverse events under product code DZM

product code DZM

Injury: 139
Total: 139

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.