HAMACHER BULLET POINT OPHTHALMIC NEEDLE— 510(k) K872200

Name: FDA 510(k) clearance K872200
Creator: U.S. Food and Drug Administration
Published: 1987-06-25

Substantially Equivalent

R. J. Doyle, Inc.

FDA 510(k) clearance K872200 for HAMACHER BULLET POINT OPHTHALMIC NEEDLE, Substantially Equivalent on 1987-06-25. Applicant: R. J. Doyle, Inc.. Device class: 1.

Clearance details

Applicant: R. J. Doyle, Inc.
Product code: Code HMX
Device class: Class 1
Regulation: 21 CFR 886.4350
Advisory panel: Ophthalmic
Date received: 1987-06-08
Decision date: 1987-06-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Spokane, WA, US

Download summary PDF View on FDA.gov ↗

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More clearances from R. J. Doyle, Inc.

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K894878 — 16GA X 6 BULLET POINT NEEDLE, FLEX STAINLESS STEE1989-11-30
K894879 — 16GA X 10 MIDDLE SIZE BULLET POINT NEEDLE1989-11-30
K894880 — 16GA X 14 FOURTEEN LONG LONG BULLET POINT NEEDL1989-11-30
K894881 — 20GA X 7-1/2 THREADING BULLET POINT NEEDLE1989-11-30
K894882 — INFILTRATION PUMP SYRINGE1989-11-30

Adverse events under product code HMX

product code HMX

Other: 1
Total: 1

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.