LASER CENTERING DEVICE— 510(k) K872747

Substantially Equivalent

Innomed Corp.

FDA 510(k) clearance K872747 for LASER CENTERING DEVICE, Substantially Equivalent on 1987-09-04. Applicant: Innomed Corp.. Device class: 1.

Clearance details

Applicant: Innomed Corp.
Product code: Code HMR
Device class: Class 1
Regulation: 21 CFR 886.4570
Advisory panel: Ophthalmic
Date received: 1987-07-13
Decision date: 1987-09-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Brea, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HMR

K053475 — OPTIPOINT CORNEAL MARKER, MODEL VPT-OPT-4502006-03-03
K925606 — OPTICAL ZONE/HEXAGONAL/ASTIGMATISM/RADIAL MARKERS1994-08-29
K863663 — OPHTHALMIC SURGICAL OCULAR MARKERS1986-10-20
K861535 — OPTICAL MARKERS/FIXATION RING/CANNU & IRRIGA CANNU1986-05-14

More clearances from Innomed Corp.

K822574 — INNOMED PD-1 KIT1982-10-13
K827796 — INNOSCAN EXAMINATION LIGHT1982-08-24

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