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FDA 510(k)

DIGISTORE 50

K-Number: K842191 · 1984-10-25

ApplicantVas Corp.
Decision Date1984-10-25
Product CodeJAA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DIGISTORE 50 is the device name listed in this FDA 510(k) record. The listed applicant is Vas Corp.. It received FDA 510(k) clearance on 1984-10-25 under 510(k) number K842191. The device is classified under product code JAA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIGISTORE 50?

DIGISTORE 50 is a medical device that received FDA 510(k) clearance on 1984-10-25. The listed applicant is Vas Corp.. The 510(k) number is K842191.

When did DIGISTORE 50 receive FDA 510(k) clearance?

DIGISTORE 50 received FDA 510(k) clearance on 1984-10-25, under 510(k) number K842191.

Who is the listed applicant for DIGISTORE 50?

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

What is the FDA product code for DIGISTORE 50?

The FDA product code for DIGISTORE 50 is JAA.

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Related Devices (Code: JAA)

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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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