BARRON TWIN BLADE TREPHINE FOR EPPIKARATOPHAKIA— 510(k) K860648

Name: FDA 510(k) clearance K860648
Creator: U.S. Food and Drug Administration
Published: 1986-03-25

Substantially Equivalent for Some Indications

Precision Instruments, Inc.

FDA 510(k) clearance K860648 for BARRON TWIN BLADE TREPHINE FOR EPPIKARATOPHAKIA, Substantially Equivalent for Some Indications on 1986-03-25. Applicant: Precision Instruments, Inc.. Device class: 1.

Clearance details

Applicant: Precision Instruments, Inc.
Product code: Code HRH
Device class: Class 1
Regulation: 21 CFR 886.4350
Advisory panel: Ophthalmic
Date received: 1986-02-20
Decision date: 1986-03-25
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Grand Blanc, MI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HRH

view all

K022843 — GAYHEART CORNEAL EXCISION DEVICE2002-11-01
K931792 — ARTHROSCOPE1994-06-13
K873918 — HEAD & CHIN RESTS1987-10-28
K864520 — BARRON ROTARY BLADE TREPHINE USING HESSBURG-BARRON1987-01-20
K862524 — DEKNATEL (R) TREPHINE1986-08-11

More clearances from Precision Instruments, Inc.

view all

K843048 — RING SUPPORTED TREPHINE FOR CORNEA TRANS1984-10-05
K801585 — HESSBURG-BFRRON TREPHINE1980-10-03

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