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FDA 510(k)

QUANTASCOPE

K-Number: K870442 · 1987-08-11

ApplicantVital Science Corp.
Decision Date1987-08-11
Product CodeDXR
Advisory CommitteeCV
DecisionSubstantially Equivalent for Some Indications

Device Summary

QUANTASCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Vital Science Corp.. It received FDA 510(k) clearance on 1987-08-11 under 510(k) number K870442. The device is classified under product code DXR. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the QUANTASCOPE?

QUANTASCOPE is a medical device that received FDA 510(k) clearance on 1987-08-11. The listed applicant is Vital Science Corp.. The 510(k) number is K870442.

When did QUANTASCOPE receive FDA 510(k) clearance?

QUANTASCOPE received FDA 510(k) clearance on 1987-08-11, under 510(k) number K870442.

Who is the listed applicant for QUANTASCOPE?

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

What is the FDA product code for QUANTASCOPE?

The FDA product code for QUANTASCOPE is DXR.

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Related Devices (Code: DXR)

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.

K243566CardioTag™Cardiosense, Inc.K160656CorSensCorsens Medical , Ltd.K081603DIGITAL BALLISTOCARDIOGRAPH, MODEL DGB 300Heartforce Medical, Inc.K863508FRANTZ MEDICAL ELECTRODEFrantz Medical Development, Ltd.

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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