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FDA 510(k)

VIEWSEND MEDICAL MODEL 1200

K-Number: K962225 · 1996-10-25

ApplicantKlt Telecom, Inc.
Decision Date1996-10-25
Product CodeLMD
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VIEWSEND MEDICAL MODEL 1200 is the device name listed in this FDA 510(k) record. The listed applicant is Klt Telecom, Inc.. It received FDA 510(k) clearance on 1996-10-25 under 510(k) number K962225. The device is classified under product code LMD. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIEWSEND MEDICAL MODEL 1200?

VIEWSEND MEDICAL MODEL 1200 is a medical device that received FDA 510(k) clearance on 1996-10-25. The listed applicant is Klt Telecom, Inc.. The 510(k) number is K962225.

When did VIEWSEND MEDICAL MODEL 1200 receive FDA 510(k) clearance?

VIEWSEND MEDICAL MODEL 1200 received FDA 510(k) clearance on 1996-10-25, under 510(k) number K962225.

Who is the listed applicant for VIEWSEND MEDICAL MODEL 1200?

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

What is the FDA product code for VIEWSEND MEDICAL MODEL 1200?

The FDA product code for VIEWSEND MEDICAL MODEL 1200 is LMD.

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 Klt Telecom, 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.

K013994MODIFICATION TO VIEWSEND MEDICAL

Related Devices (Code: LMD)

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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