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FDA 510(k)

INTERMEDICS TRIANGLE CHEST PROBE MODEL 526-04

K-Number: K933278 · 1995-03-15

ApplicantIntermedics, Inc.
Decision Date1995-03-15
Product CodeKRG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

INTERMEDICS TRIANGLE CHEST PROBE MODEL 526-04 is the device name listed in this FDA 510(k) record. The listed applicant is Intermedics, Inc.. It received FDA 510(k) clearance on 1995-03-15 under 510(k) number K933278. 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 INTERMEDICS TRIANGLE CHEST PROBE MODEL 526-04?

INTERMEDICS TRIANGLE CHEST PROBE MODEL 526-04 is a medical device that received FDA 510(k) clearance on 1995-03-15. The listed applicant is Intermedics, Inc.. The 510(k) number is K933278.

When did INTERMEDICS TRIANGLE CHEST PROBE MODEL 526-04 receive FDA 510(k) clearance?

INTERMEDICS TRIANGLE CHEST PROBE MODEL 526-04 received FDA 510(k) clearance on 1995-03-15, under 510(k) number K933278.

Who is the listed applicant for INTERMEDICS TRIANGLE CHEST PROBE MODEL 526-04?

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

What is the FDA product code for INTERMEDICS TRIANGLE CHEST PROBE MODEL 526-04?

The FDA product code for INTERMEDICS TRIANGLE CHEST PROBE MODEL 526-04 is KRG.

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Other records listing Intermedics, 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.

K954610MODEL 430-07 ENDOCARDIAL PACING LEADK955122INTERMEDICS MODEL 436-07 BIPOLAR & MODEL 437-07 UNIPOLAR IMPLANTABLE ENDOCARDIAL PACING LEADK962174BIPLR IM EN PAC LEADS (430-07,432-03,436-02 & 07, 438-05 & 07)K955550CARDIFIX EZ BIPOLAR/UNIPOLAR ENDOCARDIAL PACING LEADK960281IMPLANTABLE PACING LEADS/IMPLANTABLE ACCESSORY/NON-IMPLANTABLE ACCESSORYK954719INTERMEDICS MODEL 430-07 BIPOLAR IMPLANTABLE ENDOCARDIAL PACING LEAD

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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.

K884522MODEL 5650 OPTIMATE PERSONAL PROGRAMMERTeletronics, Inc.K880738MODEL 2331T PATIENT PROGRAMMERMedtronic VascularK882429MODEL 255A PROGRAMMER III, W/SOFTWARE REVI. 4004Tpl-Cordis, Inc.K864712MODEL 1740 PERSONAL POCKET PROGRAMMERTelectronics, 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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