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FDA 510(k)

VIEWSCAN

K-Number: K863994 · 1986-10-31

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

Device Summary

VIEWSCAN 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 K863994. The device is classified under product code HOT. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIEWSCAN?

VIEWSCAN 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 K863994.

When did VIEWSCAN receive FDA 510(k) clearance?

VIEWSCAN received FDA 510(k) clearance on 1986-10-31, under 510(k) number K863994.

Who is the listed applicant for VIEWSCAN?

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 VIEWSCAN?

The FDA product code for VIEWSCAN is HOT.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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 AUDIOMETERK863995KEYNOTEK863993VTS REPORTER OR VTS LINK

Related Devices (Code: HOT)

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.

K873967SPECTACLE, MAGNIFYINGSwank Plus , 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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