SUCTION REGULATOR 7700 SERIES— 510(k) K850200

Name: FDA 510(k) clearance K850200
Creator: U.S. Food and Drug Administration
Published: 1985-03-04

Substantially Equivalent

Boehringer Laboratories

FDA 510(k) clearance K850200 for SUCTION REGULATOR 7700 SERIES, Substantially Equivalent on 1985-03-04. Applicant: Boehringer Laboratories. Device class: 2.

Clearance details

Applicant: Boehringer Laboratories
Product code: Code KDP
Device class: Class 2
Regulation: 21 CFR 880.6740
Advisory panel: General Hospital
Date received: 1985-01-18
Decision date: 1985-03-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Norristown, PA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KDP

view all

K013976 — BOEHRINGER MRI SUCTION REGULATORY2002-01-08
K944479 — PM3300 INTERMITTENT VACUUM1994-12-22
K942747 — MALCOLM-LYNN(TM) EOT SUCTION REG VALVE(TM) (SRV) )1994-07-21
K933232 — BOEHRINGER LABORATORIES SUCTION REGULATOR, MODIFIED1994-03-28
K926140 — VACUUM POWER BODY FLUID SUCTION APPARATUS1993-07-27

More clearances from Boehringer Laboratories

view all

K234145 — ViSiGi 3D Gastric Sizing Tube2024-01-26
K061788 — BOEHRINGER LABORATORIES SUCTION PUMP SYSTEM2006-07-11
K060277 — BOEHRINGER LABORATORIES SUCTION PUMP SYSTEM2006-03-03
K020538 — BOEHRINGER LABORATORIES PNEUMATIC AMBULATORY COMPRESSION SYSTEM 8200 SERIES2002-05-15
K014187 — AUTOVAC ORTHOPEDIC AUTOTRANSFUSION SYSTEM2002-02-06

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