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FDA 510(k)

CERYX6, 611, CERYX 3 311 & CERYX 1 111

K-Number: K844485 · 1985-04-19

ApplicantVitatron Medical BV
Decision Date1985-04-19
Product CodeKRG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CERYX6, 611, CERYX 3 311 & CERYX 1 111 is the device name listed in this FDA 510(k) record. The listed applicant is Vitatron Medical BV. It received FDA 510(k) clearance on 1985-04-19 under 510(k) number K844485. 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 CERYX6, 611, CERYX 3 311 & CERYX 1 111?

CERYX6, 611, CERYX 3 311 & CERYX 1 111 is a medical device that received FDA 510(k) clearance on 1985-04-19. The listed applicant is Vitatron Medical BV. The 510(k) number is K844485.

When did CERYX6, 611, CERYX 3 311 & CERYX 1 111 receive FDA 510(k) clearance?

CERYX6, 611, CERYX 3 311 & CERYX 1 111 received FDA 510(k) clearance on 1985-04-19, under 510(k) number K844485.

Who is the listed applicant for CERYX6, 611, CERYX 3 311 & CERYX 1 111?

The FDA 510(k) record lists Vitatron Medical BV as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CERYX6, 611, CERYX 3 311 & CERYX 1 111?

The FDA product code for CERYX6, 611, CERYX 3 311 & CERYX 1 111 is KRG.

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Other records listing Vitatron Medical BV 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.

K854790CERYX PACEMAKER MODELS 114, 314 & 614K844484HEWLETT PACKARDT HP 85 W/ VITATRON PH1 PROGRAM HEAK844483TP 1K840668ELECTRODE PACEMAKER, PERM & TEMPK831859PACEMAKER PROGRAMMER #2032K831860GENERATOR, PULSE, PACEMAKER #532

View all 19 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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