VICKERS MEDICAL MODEL 112 TREONIC DC2
K-Number: K791645 · 1979-10-02
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Device Summary
Frequently Asked Questions
What is the VICKERS MEDICAL MODEL 112 TREONIC DC2?
VICKERS MEDICAL MODEL 112 TREONIC DC2 is a medical device that received FDA 510(k) clearance on 1979-10-02. The listed applicant is Vickers America Medical Corp.. The 510(k) number is K791645.
When did VICKERS MEDICAL MODEL 112 TREONIC DC2 receive FDA 510(k) clearance?
VICKERS MEDICAL MODEL 112 TREONIC DC2 received FDA 510(k) clearance on 1979-10-02, under 510(k) number K791645.
Who is the listed applicant for VICKERS MEDICAL MODEL 112 TREONIC DC2?
The FDA 510(k) record lists Vickers America Medical Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VICKERS MEDICAL MODEL 112 TREONIC DC2?
The FDA product code for VICKERS MEDICAL MODEL 112 TREONIC DC2 is FKW.
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 Vickers America Medical 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: FKW)
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
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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