SILGEL STC-S
K-Number: K984029 · 1999-08-05
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Device Summary
Frequently Asked Questions
What is the SILGEL STC-S?
SILGEL STC-S is a medical device that received FDA 510(k) clearance on 1999-08-05. The listed applicant is Nagor , Ltd.. The 510(k) number is K984029.
When did SILGEL STC-S receive FDA 510(k) clearance?
SILGEL STC-S received FDA 510(k) clearance on 1999-08-05, under 510(k) number K984029.
Who is the listed applicant for SILGEL STC-S?
The FDA 510(k) record lists Nagor , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SILGEL STC-S?
The FDA product code for SILGEL STC-S is MDA.
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 Nagor , 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.
Related Devices (Code: MDA)
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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