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FDA 510(k)

MODEL 1740 PERSONAL POCKET PROGRAMMER

K-Number: K864712 · 1987-12-17

ApplicantTelectronics, Inc.
Decision Date1987-12-17
Product CodeKRG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODEL 1740 PERSONAL POCKET PROGRAMMER is the device name listed in this FDA 510(k) record. The listed applicant is Telectronics, Inc.. It received FDA 510(k) clearance on 1987-12-17 under 510(k) number K864712. The device is classified under product code KRG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 1740 PERSONAL POCKET PROGRAMMER?

MODEL 1740 PERSONAL POCKET PROGRAMMER is a medical device that received FDA 510(k) clearance on 1987-12-17. The listed applicant is Telectronics, Inc.. The 510(k) number is K864712.

When did MODEL 1740 PERSONAL POCKET PROGRAMMER receive FDA 510(k) clearance?

MODEL 1740 PERSONAL POCKET PROGRAMMER received FDA 510(k) clearance on 1987-12-17, under 510(k) number K864712.

Who is the listed applicant for MODEL 1740 PERSONAL POCKET PROGRAMMER?

The FDA 510(k) record lists Telectronics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL 1740 PERSONAL POCKET PROGRAMMER?

The FDA product code for MODEL 1740 PERSONAL POCKET PROGRAMMER is KRG.

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Other records listing Telectronics, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K890895IMPLANTABLE ADAPTOR 033-380K891231OPTIMA MPT AND SPT PACEMAKERSK890350VS-1 SILICONE IMPLANT LEADS (NEW SERIAL # TUBE)K884411OPTIMA MPT AND SPT PACEMAKERSK884278IMPLANTABLE ELECTRODE LEADS 033-400,402 AND 436K881837OPTIMA MPT SERIES III PACEMAKER, 5281D AND 5282D

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Related Devices (Code: KRG)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K933278INTERMEDICS TRIANGLE CHEST PROBE MODEL 526-04Intermedics, Inc.K884522MODEL 5650 OPTIMATE PERSONAL PROGRAMMERTeletronics, Inc.K880738MODEL 2331T PATIENT PROGRAMMERMedtronic VascularK882429MODEL 255A PROGRAMMER III, W/SOFTWARE REVI. 4004Tpl-Cordis, Inc.K871986MODEL 5600B PROGRAMMER, PACEMAKERTelectronics, Inc.K863046ULTRA SOFTWARE MODULE: MODEL 2016Cardiac Pacemakers, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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