MENTOR(R) DURASTAT(TM) AUTOCLAV BIPOLAR HEMOSTAT— 510(k) K903878

Name: FDA 510(k) clearance K903878
Creator: U.S. Food and Drug Administration
Published: 1990-11-05

Substantially Equivalent

Mentor O & O, Inc.

FDA 510(k) clearance K903878 for MENTOR(R) DURASTAT(TM) AUTOCLAV BIPOLAR HEMOSTAT, Substantially Equivalent on 1990-11-05. Applicant: Mentor O & O, Inc.. Device class: 2.

Clearance details

Applicant: Mentor O & O, Inc.
Product code: Code HQQ
Device class: Class 2
Regulation: 21 CFR 886.4100
Advisory panel: Ophthalmic
Date received: 1990-08-22
Decision date: 1990-11-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Norwell, MA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HQQ

view all

K910088 — SCITECH BI-MANUAL ADAPTER CLIPS1991-04-08
K881001 — MENTOR WET-FIELD*II COAGULATOR1988-05-13

More clearances from Mentor O & O, Inc.

view all

K955245 — MENTOR MERIDIAN PHACOEMULSIFICATION SYSTEM1996-02-12
K934320 — MENTOR WET-FIELD HEMOSTATIC ERASER BIPOLAR INSTRUMENT, 20 GAUGE WITH EXTRUSION ASPIRATION1994-02-16
K912904 — MENTOR ODYSSEY PHACOEMULSIFICATION SYSTEM1992-06-11
K915340 — MENTOR HORIZON LOW VISION MAGNIFIER1992-03-30
K910637 — MENTOR(R) SUR-E-TROL(R)1991-05-13

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