PRESSURE MONITOR, MODEL 1131B— 510(k) K801110

Name: FDA 510(k) clearance K801110
Creator: U.S. Food and Drug Administration
Published: 1980-05-20

Substantially Equivalent

American Optical Corp.

FDA 510(k) clearance K801110 for PRESSURE MONITOR, MODEL 1131B, Substantially Equivalent on 1980-05-20. Applicant: American Optical Corp.. Device class: 2.

Clearance details

Applicant: American Optical Corp.
Product code: Code DSK
Device class: Class 2
Regulation: 21 CFR 870.1110
Advisory panel: Cardiovascular
Date received: 1980-05-12
Decision date: 1980-05-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code DSK

view all

K231586 — Endophys Blood Pressure Monitor model BPM-302023-11-03
K160945 — Endophys Blood Pressure Monitor2016-09-26
K152582 — CORE FM System, Patient Interface Module (OPIM), Hemodynamic Converter Box2015-12-03
K141615 — ENDOPHYS BLOOD PRESSURE MONITOR2015-01-07
K080670 — MODIFICATION TO SPHYGMOCOR CARDIOVASCULAR MANAGEMENT SYSTEM2008-04-23

More clearances from American Optical Corp.

view all

K950881 — PHACO TIP1995-09-06
K950880 — AOI UNIVERSAL ULTRASONIC HANDPIECE1995-05-26
K931354 — P4000 PHACOEMULSIFIER1994-02-22
K931358 — AORP4000 REUSABLE PAK1994-02-22
K931357 — AOD4000 DISPOSABLE PAK1994-01-25

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