Cleared Traditional

K953107 - ANESTHESIA/RESPIRATORY FACE MASK

K953107 is an FDA 510(k) clearance for ANESTHESIA/RESPIRATORY FACE MASK, manufactured by Medical Marketing Concepts. The device is a Class 1 Anesthesiology device with product code BSJ cleared through the Traditional 510(k) pathway after a 43-day FDA review.

K953107 · Medical Marketing Concepts · Anesthesiology device
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Aug 1995
Decision
43d
Days
Class 1
Risk

K953107 is an FDA 510(k) clearance for the ANESTHESIA/RESPIRATORY FACE MASK. Classified as Mask, Gas, Anesthetic (product code BSJ), Class I - General Controls.

Submitted by Medical Marketing Concepts (Hardy, US). The FDA issued a Cleared decision on August 15, 1995 after a review of 43 days - a notably fast clearance cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.5550 - 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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Medical Marketing Concepts devices

FDA 510(k) Submission Details - K953107

510(k) Number K953107 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 03, 1995
Decision Date August 15, 1995
Days to Decision 43 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
97d faster than avg
Panel avg: 140d · This submission: 43d
Pathway characteristics
Predicate-based equivalence.

BSJ Device Classification - Class 1, General Controls

Product Code BSJ Mask, Gas, Anesthetic
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 868.5550
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 - BSJ Mask, Gas, Anesthetic

All 29
Devices cleared under the same product code (BSJ) and FDA review panel - the closest regulatory comparables to K953107.
ANESTHESIA FACE MASK
K953295 · Mallinckrodt Medical · Aug 1995
AIR-SOFT-DISPOSABLE, ANESTHESISA/RESPIRATORY FACE MASK
K951043 · Promedic, Inc. · Jun 1995
AMBU DISPOSABLE FACE MASK
K932014 · Ambu, Inc. · Jun 1993
VENTLAB VENT-MASK, CAT# VR 0010/20/30
K903881 · Ventlab Corp. · Sep 1990
ANESTHESIA/RESPIRATORY DISPOSABLE MASK
K891316 · Concord/Portex · Aug 1989
RESPIRONICS SEALEASY II
K890795 · Respironics, Inc. · Apr 1989