POSTERIOR CAPSULOTOMY CYSTITOME— 510(k) K840660

Name: FDA 510(k) clearance K840660
Creator: U.S. Food and Drug Administration
Published: 1984-03-16

Substantially Equivalent

Sharpoint, Inc.

FDA 510(k) clearance K840660 for POSTERIOR CAPSULOTOMY CYSTITOME, Substantially Equivalent on 1984-03-16. Applicant: Sharpoint, Inc.. Device class: 1.

Clearance details

Applicant: Sharpoint, Inc.
Product code: Code HNY
Device class: Class 1
Regulation: 21 CFR 886.4350
Advisory panel: Ophthalmic
Date received: 1984-02-15
Decision date: 1984-03-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K874976 — PRISMA DISPOS. DOUBLE SHARP IRRIGATING CYSTOTOME1988-04-13
K874983 — PRISMA DISPOSABLE ANGLED IRRIGATING CYSTOTOME1988-04-13

More clearances from Sharpoint, Inc.

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K863595 — COATED SUTURE NEEDLE1986-10-24
K861947 — SURGICAL KNIFE1986-06-06
K840764 — EAR KNIVES1984-05-21
K840855 — CORNEAL SCLERAL LANCE1984-05-09
K840659 — ANTERIOR CAPSULECTOMY CYSTITOME1984-03-16

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