S-SCORT...JR QUICKDRAW, MODEL 2400
K-Number: K041154 · 2004-05-18
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Device Summary
Frequently Asked Questions
What is the S-SCORT...JR QUICKDRAW, MODEL 2400?
S-SCORT...JR QUICKDRAW, MODEL 2400 is a medical device that received FDA 510(k) clearance on 2004-05-18. The listed applicant is Sscor. The 510(k) number is K041154.
When did S-SCORT...JR QUICKDRAW, MODEL 2400 receive FDA 510(k) clearance?
S-SCORT...JR QUICKDRAW, MODEL 2400 received FDA 510(k) clearance on 2004-05-18, under 510(k) number K041154.
Who is the listed applicant for S-SCORT...JR QUICKDRAW, MODEL 2400?
The FDA 510(k) record lists Sscor as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for S-SCORT...JR QUICKDRAW, MODEL 2400?
The FDA product code for S-SCORT...JR QUICKDRAW, MODEL 2400 is BTA.
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 Sscor 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: BTA)
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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