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FDA 510(k)

7100 SWALLOWING WORKSTATION

K-Number: K954798 · 1996-06-04

Decision Date1996-06-04
Product CodeKLA
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

7100 SWALLOWING WORKSTATION is the device name listed in this FDA 510(k) record. The listed applicant is Kay Elemetrics Corp.. It received FDA 510(k) clearance on 1996-06-04 under 510(k) number K954798. The device is classified under product code KLA. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 7100 SWALLOWING WORKSTATION?

7100 SWALLOWING WORKSTATION is a medical device that received FDA 510(k) clearance on 1996-06-04. The listed applicant is Kay Elemetrics Corp.. The 510(k) number is K954798.

When did 7100 SWALLOWING WORKSTATION receive FDA 510(k) clearance?

7100 SWALLOWING WORKSTATION received FDA 510(k) clearance on 1996-06-04, under 510(k) number K954798.

Who is the listed applicant for 7100 SWALLOWING WORKSTATION?

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

What is the FDA product code for 7100 SWALLOWING WORKSTATION?

The FDA product code for 7100 SWALLOWING WORKSTATION is KLA.

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.

Other records listing Kay Elemetrics 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.

Related Devices (Code: KLA)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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