FDA 510(k)

VISI-SPOT

K-Number: K932752 · 1993-11-05

Decision Date1993-11-05

Product CodeJTO

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

VISI-SPOT is the device name listed in this FDA 510(k) record. The listed applicant is J.S. Medical Assoc.. It received FDA 510(k) clearance on 1993-11-05 under 510(k) number K932752. The device is classified under product code JTO. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VISI-SPOT?

VISI-SPOT is a medical device that received FDA 510(k) clearance on 1993-11-05. The listed applicant is J.S. Medical Assoc.. The 510(k) number is K932752.

When did VISI-SPOT receive FDA 510(k) clearance?

VISI-SPOT received FDA 510(k) clearance on 1993-11-05, under 510(k) number K932752.

Who is the listed applicant for VISI-SPOT?

The FDA 510(k) record lists J.S. Medical Assoc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VISI-SPOT?

The FDA product code for VISI-SPOT is JTO.

Other records listing J.S. Medical Assoc. 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.

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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.