Cleared Traditional

K851805 - LPA-3 PRINTER

K851805 is an FDA 510(k) clearance for LPA-3 PRINTER, manufactured by Life Products, Inc.. The device is a Class 2 Anesthesiology device with product code BZC cleared through the Traditional 510(k) pathway after a 69-day FDA review.

K851805 · Life Products, Inc. · Anesthesiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jul 1985
Decision
69d
Days
Class 2
Risk

K851805 is an FDA 510(k) clearance for the LPA-3 PRINTER. Classified as Calculator, Pulmonary Function Data (product code BZC), Class II - Special Controls.

Submitted by Life Products, Inc. (Boulder, US). The FDA issued a Cleared decision on July 8, 1985 after a review of 69 days - a notably fast clearance cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.1880 - 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 Life Products, Inc. devices

FDA 510(k) Submission Details - K851805

510(k) Number K851805 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 30, 1985
Decision Date July 08, 1985
Days to Decision 69 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
71d faster than avg
Panel avg: 140d · This submission: 69d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

BZC Device Classification - Class 2, Special Controls

Product Code BZC Calculator, Pulmonary Function Data
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.1880
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 - BZC Calculator, Pulmonary Function Data

All 49
Devices cleared under the same product code (BZC) and FDA review panel - the closest regulatory comparables to K851805.
Q-PLEX 1
K881235 · Quinton, Inc. · Mar 1989
STAR CALC
K875027 · Infrasonics Corp. · Aug 1988
ALVEO-DIFFUSION TEST
K853443 · Erich Jaeger, Inc. · Feb 1986
OXYSCREEN
K843860 · Erich Jaeger, Inc. · Dec 1984
AW TEST
K843848 · Erich Jaeger, Inc. · Nov 1984
APTA-BRONCHOSCREEN
K843852 · Erich Jaeger, Inc. · Nov 1984