Cleared Traditional

K862462 - LIFESCOPE 6

K862462 is an FDA 510(k) clearance for LIFESCOPE 6, manufactured by Nihon Kohden America, Inc.. The device is a Class 2 Anesthesiology device with product code BZQ cleared through the Traditional 510(k) pathway after a 218-day FDA review.

K862462 · Nihon Kohden America, Inc. · Anesthesiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Feb 1987
Decision
218d
Days
Class 2
Risk

K862462 is an FDA 510(k) clearance for the LIFESCOPE 6, OEC-6120 PORTABLE PATIENT MONITOR REC. Classified as Monitor, Breathing Frequency (product code BZQ), Class II - Special Controls.

Submitted by Nihon Kohden America, Inc. (Irvine, US). The FDA issued a Cleared decision on February 3, 1987 after a review of 218 days - an extended review cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.2375 - 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 Nihon Kohden America, Inc. devices

FDA 510(k) Submission Details - K862462

510(k) Number K862462 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 30, 1986
Decision Date February 03, 1987
Days to Decision 218 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
78d slower than avg
Panel avg: 140d · This submission: 218d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

BZQ Device Classification - Class 2, Special Controls

Product Code BZQ Monitor, Breathing Frequency
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.2375
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 Anesthesiology devices follow this clearance model.

Regulatory Peers - BZQ Monitor, Breathing Frequency

All 77
Devices cleared under the same product code (BZQ) and FDA review panel - the closest regulatory comparables to K862462.
MODEL NUMBER 9216 RESPIRATION/HEART RATE MONITOR
K872954 · Aequitron Medical, Inc. · Oct 1987
MODEL NUMBER 8200 RESPIRATION/HEART RATE MONITOR
K871551 · Aequitron Medical, Inc. · Jun 1987
LIFEWATCH PLUS
K870661 · The Perkin-Elmer Corp. · Mar 1987
KONTRON VITALMON 5010 PATIENT MONITOR
K852249 · Kontron Instruments, Inc. · Oct 1986
MONAGHAN RVM, MODEL 760 AND 761
K863612 · Monaghan Medical Corp. · Oct 1986
BIOCHEM 515 RESPIRATION MONITOR
K854333 · Biochem International, Inc. · May 1986