Cleared Traditional

K822033 - BERMAN ANGIOGRAPHIC BALLOON CATHETER

K822033 is the FDA 510(k) clearance for BERMAN ANGIOGRAPHIC BALLOON CATHETER by Ziehm International, Inc.. It is a Class 2 Cardiovascular device (product code DQO) cleared through the Traditional 510(k) pathway after a 43-day FDA review.

K822033 · Ziehm International, Inc. · Cardiovascular device
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Aug 1982
Decision
43d
Days
Class 2
Risk

K822033 is an FDA 510(k) clearance for the BERMAN ANGIOGRAPHIC BALLOON CATHETER. Classified as Catheter, Intravascular, Diagnostic (product code DQO), Class II - Special Controls.

Submitted by Ziehm International, Inc. (Annapolis, US). The FDA issued a Cleared decision on August 24, 1982 after a review of 43 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.1200 - the FDA cardiovascular device oversight 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 Ziehm International, Inc. devices

Submission Details

510(k) Number K822033 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 12, 1982
Decision Date August 24, 1982
Days to Decision 43 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
82d faster than avg
Panel avg: 125d · This submission: 43d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code DQO Catheter, Intravascular, Diagnostic
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.1200
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 Cardiovascular devices follow this clearance model.

Regulatory Peers - DQO Catheter, Intravascular, Diagnostic

All 296
Devices cleared under the same product code (DQO) and FDA review panel - the closest regulatory comparables to K822033.
BRACHIAL CORONARY GUIDING CATHETER
K822862 · Advanced Cardiovascular Systems, Inc. · Oct 1982
CORONARY INFUSION KIT
K822640 · Mallinckrodt Critical Care · Sep 1982
ANGIOGRAPHIC CATHETER
K821816 · Medi-Tech, Inc. · Aug 1982
ANGIOGRAPHY KIT
K821976 · Mallinckrodt Critical Care · Jul 1982
CORONARY INFUSION KIT
K820001 · Mallinckrodt Critical Care · Jan 1982
GANZ CORONARY REPERFUSION CATHETER
K803270 · American Edwards Laboratories · Mar 1981