Cleared Traditional

K933048 - LAERDAL(TM) POCKET MASK, MODIFICATION

K933048 is an FDA 510(k) clearance for LAERDAL(TM) POCKET MASK, manufactured by Laerdal Medical Corp.. The device is a Class 1 Anesthesiology device with product code KGB cleared through the Traditional 510(k) pathway after a 205-day FDA review.

K933048 · Laerdal Medical Corp. · Anesthesiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Dec 1993
Decision
205d
Days
Class 1
Risk

K933048 is an FDA 510(k) clearance for the LAERDAL(TM) POCKET MASK, MODIFICATION. Classified as Mask, Oxygen, Non-rebreathing (product code KGB), Class I - General Controls.

Submitted by Laerdal Medical Corp. (Armonk, US). The FDA issued a Cleared decision on December 2, 1993 after a review of 205 days - an extended review cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.5570 - the FDA anesthesiology and respiratory 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 Anesthesiology review framework, consistent with the majority of Class II 510(k) submissions.

View all Laerdal Medical Corp. devices

FDA 510(k) Submission Details - K933048

510(k) Number K933048 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 11, 1993
Decision Date December 02, 1993
Days to Decision 205 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
65d slower than avg
Panel avg: 140d · This submission: 205d
Pathway characteristics
Predicate-based equivalence.

KGB Device Classification - Class 1, General Controls

Product Code KGB Mask, Oxygen, Non-rebreathing
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 868.5570
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - KGB Mask, Oxygen, Non-rebreathing

Devices cleared under the same product code (KGB) and FDA review panel - the closest regulatory comparables to K933048.
ULTIMATE SEAL
K960401 · Hans Rudolph, Inc. · Jun 1996
CHALLENGE POWDER-FREE, HYPOALLERGENIC, SYNTHETIC SURGICAL GLOVES
K935917 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Feb 1994
COMPACT MASK
K932347 · Vital Signs, Inc. · Jan 1994
OXYGEN MASK W/RESERVOIR BAG
K790161 · Airlife, Inc. · Apr 1979
OXYGEN MASK, CONCENTRATION AEROSOL MASK
K790162 · Airlife, Inc. · Apr 1979