Cleared Traditional

K882434 - MASK, GAS, ANESTHETIC

K882434 is an FDA 510(k) clearance for MASK, manufactured by Eastmed Enterprises, Inc.. The device is a Class 1 Anesthesiology device with product code BSJ cleared through the Traditional 510(k) pathway after a 16-day FDA review.

K882434 · Eastmed Enterprises, Inc. · Anesthesiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jun 1988
Decision
16d
Days
Class 1
Risk

K882434 is an FDA 510(k) clearance for the MASK, GAS, ANESTHETIC. Classified as Mask, Gas, Anesthetic (product code BSJ), Class I - General Controls.

Submitted by Eastmed Enterprises, Inc. (Marlton, US). The FDA issued a Cleared decision on June 30, 1988 after a review of 16 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 Eastmed Enterprises, Inc. devices

FDA 510(k) Submission Details - K882434

510(k) Number K882434 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 14, 1988
Decision Date June 30, 1988
Days to Decision 16 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
124d faster than avg
Panel avg: 140d · This submission: 16d
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 31
Devices cleared under the same product code (BSJ) and FDA review panel - the closest regulatory comparables to K882434.
RESPIRONICS SEALEASY II
K890795 · Respironics, Inc. · Apr 1989
MODIFIED CUSHION-FLEX(TM)
K890108 · Life Design Systems, Inc. · Jan 1989
CUSHION FLEX(TM)
K884387 · Life Design Systems, Inc. · Nov 1988
MASK, ANESTH. INFLATABLE & PEDIATRIC SCENTED, DISP
K880682 · King Systems Corp. · Mar 1988
SEALFLEX MASK
K874746 · Engineered Medical Systems · Dec 1987
RIBBED CUSHION MASK
K871851 · Engineered Medical Systems · Jun 1987