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FDA 510(k)

V2

K-Number: K970481 · 1997-07-01

ApplicantSurvivalink Corp.
Decision Date1997-07-01
Product CodeLDD
Advisory CommitteeCV
DecisionSubstantially Equivalent - Subject to Tracking Reg.

Device Summary

V2 is the device name listed in this FDA 510(k) record. The listed applicant is Survivalink Corp.. It received FDA 510(k) clearance on 1997-07-01 under 510(k) number K970481. The device is classified under product code LDD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent - Subject to Tracking Reg..

Frequently Asked Questions

What is the V2?

V2 is a medical device that received FDA 510(k) clearance on 1997-07-01. The listed applicant is Survivalink Corp.. The 510(k) number is K970481.

When did V2 receive FDA 510(k) clearance?

V2 received FDA 510(k) clearance on 1997-07-01, under 510(k) number K970481.

Who is the listed applicant for V2?

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

What is the FDA product code for V2?

The FDA product code for V2 is LDD.

Other records listing Survivalink Corp. 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.

K011901FIRSTSAVE STAR BIPHASIC, MODEL 9210/9200K010214FIRSTSAVE BIPHASIC MODEL #9200 AND 9210K993072SURVIVALINK MULTIFUNCTIONAL ELECTRODE (SVL-9630)K982264FIRSTSAVE BIPHASIC MODELS 9200 AND 9210K971149SVL-9130 DEFIBRILLATION ELECTRODEK940445VIVALINK AED DEFIBRILLATOR

View all 7 devices →

Related Devices (Code: LDD)

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.

K203231Switched Internal PaddlesPhilips North America, LLCK200849Tempus LS - ManualRemote Diagnostic Technologies, Ltd. A Philips CompanyK182503Sterilizable Internal Defibrillation Paddles for use with LIFEPAK defibrillators/monitorsPhysio-Control, Inc.K103651CARDIOMEDCardio Medical Products, Inc.K103783EURO DEFI PADS ADULT; EURO DEFI PADS ADULT RADIOTRANSPARENT: EURO DEFI PADS PEDIATRICFiab SpaK103334CARDIO MEDCardio Medical Products, 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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