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FDA 510(k)

VA 1000

K-Number: K791380 · 1979-09-19

ApplicantVitatron Medical BV
Decision Date1979-09-19
Product CodeDTA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VA 1000 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 1979-09-19 under 510(k) number K791380. The device is classified under product code DTA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VA 1000?

VA 1000 is a medical device that received FDA 510(k) clearance on 1979-09-19. The listed applicant is Vitatron Medical BV. The 510(k) number is K791380.

When did VA 1000 receive FDA 510(k) clearance?

VA 1000 received FDA 510(k) clearance on 1979-09-19, under 510(k) number K791380.

Who is the listed applicant for VA 1000?

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 VA 1000?

The FDA product code for VA 1000 is DTA.

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 HEAK844485CERYX6, 611, CERYX 3 311 & CERYX 1 111K844483TP 1K840668ELECTRODE PACEMAKER, PERM & TEMPK831860GENERATOR, PULSE, PACEMAKER #532

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Related Devices (Code: DTA)

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.

K163008CareLink SmartSync Device Manager - Pacing System AnalyzerMedtronic, Inc.K101982MERLIN PSA PATIENT CABLE EX 3150, CABLE ADAPTER EX3170, M ADAPTER EX3180St Jude Medical, CrmdK073230MODELS ERA 300 AND 3105 PACING SYSTEM ANALYZERSBiotronik, Inc.K050884ADAPTER CABLERemington Medical, Inc.K033613MODIFICATION TO ERA 300 DUAL CHAMBER PACING SYSTEM ANALYZERBiotronik, Inc.K022360ERA 3000; PA-2 IS-1 ADAPTER; EK-4-N PACEMAKER TEST CABLE; ERA 3000 CHARGER; ERA 3000 BATTERY (TYPE 2); NK-11 POWER SUPP.Biotronik, 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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