Cleared Traditional

K851230 - GAMBRO PRESSURE MONITOR GUARDS

K851230 is an FDA 510(k) clearance for GAMBRO PRESSURE MONITOR GUARDS, manufactured by Gambro, Inc.. The device is a Class 2 Gastroenterology & Urology device with product code FIB cleared through the Traditional 510(k) pathway after a 14-day FDA review.

K851230 · Gambro, Inc. · Gastroenterology & Urology device
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Apr 1985
Decision
14d
Days
Class 2
Risk

K851230 is an FDA 510(k) clearance for the GAMBRO PRESSURE MONITOR GUARDS. Classified as Protector, Transducer, Dialysis (product code FIB), Class II - Special Controls.

Submitted by Gambro, Inc. (Lincolnshire, US). The FDA issued a Cleared decision on April 9, 1985 after a review of 14 days - a notably fast clearance cycle.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.5820 - the FDA gastroenterology and urology 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 Gambro, Inc. devices

FDA 510(k) Submission Details - K851230

510(k) Number K851230 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 26, 1985
Decision Date April 09, 1985
Days to Decision 14 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
116d faster than avg
Panel avg: 130d · This submission: 14d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FIB Device Classification - Class 2, Special Controls

Product Code FIB Protector, Transducer, Dialysis
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.5820
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 Gastroenterology & Urology devices follow this clearance model.

Regulatory Peers - FIB Protector, Transducer, Dialysis

All 12
Devices cleared under the same product code (FIB) and FDA review panel - the closest regulatory comparables to K851230.
MILLEX, DUALEX (PLUS, ULTRA)
K934069 · Millipore Corp. · Apr 1994
TRANSDUCER PROTECTOR
K910821 · Gelman Sciences, Inc. · Aug 1991
DA-46 FLUID BARRIER
K891752 · Akcess Medical Products, Inc. · Apr 1989
TRANSDUCER FILTER
K821268 · Cp Medical · Jun 1982
BACTASHIELD
K811859 · Tri-Med, Inc. · Aug 1981
CORDIS DOW SERA FLO TM TRANSDUCER PROT
K811892 · Cordis Corp. · Jul 1981