Cleared Traditional

K030271 - VENTLAB BACTERIAL FILTER

K030271 is an FDA 510(k) clearance for VENTLAB BACTERIAL FILTER, manufactured by Ventlab Corp.. The device is a Class 2 General Hospital device with product code CAH cleared through the Traditional 510(k) pathway after a 161-day FDA review.

K030271 · Ventlab Corp. · General Hospital
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Jul 2003
Decision
161d
Days
Class 2
Risk

K030271 is an FDA 510(k) clearance for the VENTLAB BACTERIAL FILTER, MODEL BF100. Classified as Filter, Bacterial, Breathing-circuit (product code CAH), Class II - Special Controls.

Submitted by Ventlab Corp. (Mocksville, US). The FDA issued a Cleared decision on July 7, 2003 after a review of 161 days - an extended review cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 868.5260 - the FDA general hospital device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the General Hospital review framework, consistent with the majority of Class II 510(k) submissions.

View all Ventlab Corp. devices

FDA 510(k) Submission Details - K030271

510(k) Number K030271 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 27, 2003
Decision Date July 07, 2003
Days to Decision 161 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
32d slower than avg
Panel avg: 129d · This submission: 161d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

CAH Device Classification - Class 2, Special Controls

Product Code CAH Filter, Bacterial, Breathing-circuit
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.5260
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most General Hospital devices follow this clearance model.

Regulatory Peers - CAH Filter, Bacterial, Breathing-circuit

All 81
Devices cleared under the same product code (CAH) and FDA review panel - the closest regulatory comparables to K030271.
HUMID-VENT HEPA
K112958 · Teleflex Medical · Sep 2012
RT019 INSPIRATORY/EXPIRATORY FILTER
K050927 · Fisher &Paykel Healthcare , Ltd. · Aug 2005
MIN-FILTER/S, UNI-FILTER JUNIOR, UNI-FILTER/S ANGLED AND UNI-FILTER
K043120 · Datex-Ohmeda, Inc. · Mar 2005
DATEX-OHMEDA MINI-FILTER/S AND UNI-FILTER JUNIOR
K030990 · Datex-Ohmeda · Jun 2003
DATEX-OHMEDA HMEF 750
K031653 · Datex-Ohmeda · Jun 2003
DATEX-OHMEDA HMEF MINI
K023641 · Datex-Ohmeda · Nov 2002