STRYKERSCOPE TM/ORTHOSCOPE TM/STRYKER MINISCOPE TM— 510(k) K871816

Name: FDA 510(k) clearance K871816
Creator: U.S. Food and Drug Administration
Published: 1987-08-03

Substantially Equivalent

Stryker Corp.

FDA 510(k) clearance K871816 for STRYKERSCOPE TM/ORTHOSCOPE TM/STRYKER MINISCOPE TM, Substantially Equivalent on 1987-08-03. Applicant: Stryker Corp.. Device class: 1.

Clearance details

Applicant: Stryker Corp.
Product code: Code EAY
Device class: Class 1
Regulation: 21 CFR 872.4620
Advisory panel: Dental
Date received: 1987-05-11
Decision date: 1987-08-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kalamazoo, MI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code EAY

view all

K953191 — MODEL A15-1011995-09-05
K953192 — MODEL A15-1031995-09-05
K935718 — JEDENTAL VLC DENTAL CURING LIGHT1994-01-26
K831976 — POWER OPTIC1983-08-12
K831824 — DENTAL ELECTRONIC/S.B.R TRADING BU HAND1983-08-11

More clearances from Stryker Corp.

view all

K230045 — HipCheck2023-09-29
K191259 — Stryker CrossFlow Integrated Arthroscopy Pump2019-07-12
K182359 — HipCheck2018-12-13
K143399 — Stryker Footed Attachments and Cutting Accessories2015-05-08
K143320 — Stryker Elite Attachments, Stryker Heavy Duty (HD) Attachments2015-04-23

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