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FDA 510(k)

VTS REPORTER OR VTS LINK

K-Number: K863993 · 1986-10-31

ApplicantSensory Aids Corp.
Decision Date1986-10-31
Product CodeHPF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

VTS REPORTER OR VTS LINK is the device name listed in this FDA 510(k) record. The listed applicant is Sensory Aids Corp.. It received FDA 510(k) clearance on 1986-10-31 under 510(k) number K863993. The device is classified under product code HPF. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VTS REPORTER OR VTS LINK?

VTS REPORTER OR VTS LINK is a medical device that received FDA 510(k) clearance on 1986-10-31. The listed applicant is Sensory Aids Corp.. The 510(k) number is K863993.

When did VTS REPORTER OR VTS LINK receive FDA 510(k) clearance?

VTS REPORTER OR VTS LINK received FDA 510(k) clearance on 1986-10-31, under 510(k) number K863993.

Who is the listed applicant for VTS REPORTER OR VTS LINK?

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

What is the FDA product code for VTS REPORTER OR VTS LINK?

The FDA product code for VTS REPORTER OR VTS LINK is HPF.

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.

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Other records listing Sensory Aids 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.

K872042PLAYTONE AUDIOMETERK863995KEYNOTEK863994VIEWSCAN

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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