QS DELIVERY SYSTEM
K-Number: K991254 · 1999-08-23
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Device Summary
Frequently Asked Questions
What is the QS DELIVERY SYSTEM?
QS DELIVERY SYSTEM is a medical device that received FDA 510(k) clearance on 1999-08-23. The listed applicant is Sub-Q, Inc.. The 510(k) number is K991254.
When did QS DELIVERY SYSTEM receive FDA 510(k) clearance?
QS DELIVERY SYSTEM received FDA 510(k) clearance on 1999-08-23, under 510(k) number K991254.
Who is the listed applicant for QS DELIVERY SYSTEM?
The FDA 510(k) record lists Sub-Q, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for QS DELIVERY SYSTEM?
The FDA product code for QS DELIVERY SYSTEM is KYZ.
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 Sub-Q, Inc. 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: KYZ)
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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