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FDA 510(k)

INTERMEDICS PROGRAMMER, MODEL 522-03

K-Number: K812813 · 1981-10-27

ApplicantIntermedics, Inc.
Decision Date1981-10-27
Product CodeKRG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

INTERMEDICS PROGRAMMER, MODEL 522-03 is the device name listed in this FDA 510(k) record. The listed applicant is Intermedics, Inc.. It received FDA 510(k) clearance on 1981-10-27 under 510(k) number K812813. 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 PROGRAMMER, MODEL 522-03?

INTERMEDICS PROGRAMMER, MODEL 522-03 is a medical device that received FDA 510(k) clearance on 1981-10-27. The listed applicant is Intermedics, Inc.. The 510(k) number is K812813.

When did INTERMEDICS PROGRAMMER, MODEL 522-03 receive FDA 510(k) clearance?

INTERMEDICS PROGRAMMER, MODEL 522-03 received FDA 510(k) clearance on 1981-10-27, under 510(k) number K812813.

Who is the listed applicant for INTERMEDICS PROGRAMMER, MODEL 522-03?

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 PROGRAMMER, MODEL 522-03?

The FDA product code for INTERMEDICS PROGRAMMER, MODEL 522-03 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

View all 211 devices →

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.K864712MODEL 1740 PERSONAL POCKET PROGRAMMERTelectronics, Inc.K871986MODEL 5600B PROGRAMMER, PACEMAKERTelectronics, 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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