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FDA 510(k)

WRITESTAR, AND VIEWSTAR

K-Number: K964274 · 1997-01-10

ApplicantComview Corp.
Decision Date1997-01-10
Product CodeLMB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

WRITESTAR, AND VIEWSTAR is the device name listed in this FDA 510(k) record. The listed applicant is Comview Corp.. It received FDA 510(k) clearance on 1997-01-10 under 510(k) number K964274. The device is classified under product code LMB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WRITESTAR, AND VIEWSTAR?

WRITESTAR, AND VIEWSTAR is a medical device that received FDA 510(k) clearance on 1997-01-10. The listed applicant is Comview Corp.. The 510(k) number is K964274.

When did WRITESTAR, AND VIEWSTAR receive FDA 510(k) clearance?

WRITESTAR, AND VIEWSTAR received FDA 510(k) clearance on 1997-01-10, under 510(k) number K964274.

Who is the listed applicant for WRITESTAR, AND VIEWSTAR?

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

What is the FDA product code for WRITESTAR, AND VIEWSTAR?

The FDA product code for WRITESTAR, AND VIEWSTAR is LMB.

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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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