Hamacher Bullet Point Ophthalmic Needle

FDA 510(k) K872200 · R. J. Doyle, Inc.

Substantially Equivalent

510(k) numberK872200

Submission

Device name
Hamacher Bullet Point Ophthalmic Needle
Applicant
R. J. Doyle, Inc.
Spokane, WA, US
Received
June 8, 1987
Decision date
June 25, 1987
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
HMX – Cannula, Ophthalmic
Device class
Class I (low risk)
Regulation
21 CFR 886.4350
Specialty
Ophthalmic

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Questions and answers

When was Hamacher Bullet Point Ophthalmic Needle cleared by the FDA?

Hamacher Bullet Point Ophthalmic Needle (K872200) received a 510(k) decision of Substantially Equivalent on June 25, 1987, 17 days after the submission was received.

What is the product code of K872200?

The FDA product code is HMX – Cannula, Ophthalmic, a Class I (low risk) device regulated under 21 CFR 886.4350.