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FDA 510(k)

SMART SPOT

K-Number: K961307 · 1996-07-01

ApplicantCmt Medical Technologies, Ltd.
Decision Date1996-07-01
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SMART SPOT is the device name listed in this FDA 510(k) record. The listed applicant is Cmt Medical Technologies, Ltd.. It received FDA 510(k) clearance on 1996-07-01 under 510(k) number K961307. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SMART SPOT?

SMART SPOT is a medical device that received FDA 510(k) clearance on 1996-07-01. The listed applicant is Cmt Medical Technologies, Ltd.. The 510(k) number is K961307.

When did SMART SPOT receive FDA 510(k) clearance?

SMART SPOT received FDA 510(k) clearance on 1996-07-01, under 510(k) number K961307.

Who is the listed applicant for SMART SPOT?

The FDA 510(k) record lists Cmt Medical Technologies, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SMART SPOT?

The FDA product code for SMART SPOT is LLZ.

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Other records listing Cmt Medical Technologies, Ltd. 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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Related Devices (Code: LLZ)

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.

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