Cleared Traditional

K782162 - BATTERY CHARGER

K782162 is an FDA 510(k) clearance for BATTERY CHARGER, manufactured by Telectronics, Inc.. The device is a Class 3 Radiology device with product code DXY cleared through the Traditional 510(k) pathway after a 215-day FDA review.

K782162 · Telectronics, Inc. · Radiology device
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Jul 1979
Decision
215d
Days
Class 3
Risk

K782162 is an FDA 510(k) clearance for the BATTERY CHARGER, 171 PACEMAKER. Classified as Implantable Pacemaker Pulse-generator (product code DXY), Class III - Premarket Approval.

Submitted by Telectronics, Inc. (Mchenry, US). The FDA issued a Cleared decision on July 24, 1979 after a review of 215 days - an extended review cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 870.3610 - the FDA radiology and imaging software 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: High-complexity regulatory submission. High regulatory complexity profile. This clearance follows a standard predicate-based equivalence path within the Radiology review framework, consistent with the majority of Class II 510(k) submissions.

View all Telectronics, Inc. devices

FDA 510(k) Submission Details - K782162

510(k) Number K782162 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 21, 1978
Decision Date July 24, 1979
Days to Decision 215 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
108d slower than avg
Panel avg: 107d · This submission: 215d
Pathway characteristics
Predicate-based equivalence.

DXY Device Classification - Class 3, Premarket Approval

Product Code DXY Implantable Pacemaker Pulse-generator
Device Class Class 3 - Premarket Approval
CFR Regulation 21 CFR 870.3610
What this classification means

Class III devices typically require Premarket Approval (PMA) with clinical evidence. Clearance through 510(k) for Class III devices is granted only when substantial equivalence to a valid predicate can be established.

Regulatory Peers - DXY Implantable Pacemaker Pulse-generator

All 339
Devices cleared under the same product code (DXY) and FDA review panel - the closest regulatory comparables to K782162.
BJORK-SHILEY AORTIC GRAFT VALVE PROSTH
K791225 · Shiley, Inc. · Aug 1979
UNILITH PULSE GENERATOR
K791219 · Ela Medical, Inc. · Jul 1979
PULSE GENERATOR, MODEL 171
K782161 · Telectronics, Inc. · Jul 1979
MODELS 2411/2418 VENTRICULAR-INHIBITED
K791093 · Medtronic Vascular · Jun 1979
CARDIAC PULSE GENERATOR, 16 SERIES
K790867 · Telectronics, Inc. · May 1979
GENERATOR, 16 SERIES, MODIFIED TOP CAP
K790868 · Telectronics, Inc. · May 1979