THE INFANT FLOW SYSTEM— 510(k) K930713

Name: FDA 510(k) clearance K930713
Creator: U.S. Food and Drug Administration
Published: 1993-09-16

Substantially Equivalent

Sechrist Industries, Inc.

FDA 510(k) clearance K930713 for THE INFANT FLOW SYSTEM, Substantially Equivalent on 1993-09-16. Applicant: Sechrist Industries, Inc.. Device class: 1.

Clearance details

Applicant: Sechrist Industries, Inc.
Product code: Code CAI
Device class: Class 1
Regulation: 21 CFR 868.5240
Advisory panel: Anesthesiology
Date received: 1993-02-11
Decision date: 1993-09-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Anaheim, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code CAI

view all

K954480 — CONDENSATE COLLECTION KIT1995-12-29
K953787 — UNICOR, INC. ADULT ANESTHESIA BREATHING CIRCUIT1995-09-19
K953788 — UNICOR, INC. GAS SAMPLING LINES & CONNECTORS1995-09-19
K952014 — PRIMA ADULT TEMPERATURE MONITORING ANESTHESIA CIRCUITS1995-05-22
K952016 — PRIMA PEDIATRIC GAS SAMPLING CIRCUITS1995-05-22

More clearances from Sechrist Industries, Inc.

view all

K140559 — SECHRIST MONOPLACE HYPERBARIC OXYGEN CHAMBER2014-05-30
K100268 — SECHRIST MONOPLACE HYPERBARIC OXYGEN CHAMBER2010-04-26
K052713 — MODEL 3300E/ER MONOPLACE HYPERBARIC OXYGEN CHAMBER2005-10-28
K023745 — SECHRIST AIR/OXYGEN MIXER, MODEL 3500 CP-G2003-01-17
K993167 — MILLENNIUM INFANT VENTILATOR1999-11-10

Adverse events under product code CAI

product code CAI

Malfunction: 869
Other: 1
Total: 870

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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