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FDA 510(k)

SILGEL STC-S

K-Number: K984029 · 1999-08-05

ApplicantNagor , Ltd.
Decision Date1999-08-05
Product CodeMDA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SILGEL STC-S is the device name listed in this FDA 510(k) record. The listed applicant is Nagor , Ltd.. It received FDA 510(k) clearance on 1999-08-05 under 510(k) number K984029. The device is classified under product code MDA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

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

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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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