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FDA 510(k)

VIVAPORE 10

K-Number: K943965 · 1995-04-11

Decision Date1995-04-11
Product CodeJJH
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

VIVAPORE 10 is the device name listed in this FDA 510(k) record. The listed applicant is Vivascience, Inc.. It received FDA 510(k) clearance on 1995-04-11 under 510(k) number K943965. The device is classified under product code JJH. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIVAPORE 10?

VIVAPORE 10 is a medical device that received FDA 510(k) clearance on 1995-04-11. The listed applicant is Vivascience, Inc.. The 510(k) number is K943965.

When did VIVAPORE 10 receive FDA 510(k) clearance?

VIVAPORE 10 received FDA 510(k) clearance on 1995-04-11, under 510(k) number K943965.

Who is the listed applicant for VIVAPORE 10?

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

What is the FDA product code for VIVAPORE 10?

The FDA product code for VIVAPORE 10 is JJH.

Related Clinical Trials

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.

Other records listing Vivascience, Inc. 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.

Related Devices (Code: JJH)

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.

Official Source

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