Cleared Traditional

K812104 - SIEMENS-ELEMA PSA 376

K812104 is an FDA 510(k) clearance for SIEMENS-ELEMA PSA 376, manufactured by Siemens Corp.. The device is a Class 2 Cardiovascular device with product code DTA cleared through the Traditional 510(k) pathway after a 131-day FDA review.

K812104 · Siemens Corp. · Cardiovascular device
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Dec 1981
Decision
131d
Days
Class 2
Risk

K812104 is an FDA 510(k) clearance for the SIEMENS-ELEMA PSA 376. Classified as Tester, Pacemaker Electrode Function (product code DTA), Class II - Special Controls.

Submitted by Siemens Corp. (Mchenry, US). The FDA issued a Cleared decision on December 2, 1981 after a review of 131 days - within the typical 510(k) review window.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.3720 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Cardiovascular review framework, consistent with the majority of Class II 510(k) submissions.

View all Siemens Corp. devices

FDA 510(k) Submission Details - K812104

510(k) Number K812104 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 24, 1981
Decision Date December 02, 1981
Days to Decision 131 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
6d slower than avg
Panel avg: 125d · This submission: 131d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DTA Device Classification - Class 2, Special Controls

Product Code DTA Tester, Pacemaker Electrode Function
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.3720
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 - DTA Tester, Pacemaker Electrode Function

All 7
Devices cleared under the same product code (DTA) and FDA review panel - the closest regulatory comparables to K812104.
ADAPTER CABLE
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MODIFICATION TO ERA 300 DUAL CHAMBER PACING SYSTEM ANALYZER
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K022360 · Biotronik, Inc. · Jan 2003
VA 1000
K791380 · Vitatron Medical BV · Sep 1979
CARDIOTEST 2200
K790503 · Cardiac Pacemakers, Inc. · May 1979