KELLER VITAL SIGNS MONITOR, KMS 890+
K-Number: K990648 · 1999-08-10
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Device Summary
Frequently Asked Questions
What is the KELLER VITAL SIGNS MONITOR, KMS 890+?
KELLER VITAL SIGNS MONITOR, KMS 890+ is a medical device that received FDA 510(k) clearance on 1999-08-10. The listed applicant is Keller Medical Specialties Products, Inc.. The 510(k) number is K990648.
When did KELLER VITAL SIGNS MONITOR, KMS 890+ receive FDA 510(k) clearance?
KELLER VITAL SIGNS MONITOR, KMS 890+ received FDA 510(k) clearance on 1999-08-10, under 510(k) number K990648.
Who is the listed applicant for KELLER VITAL SIGNS MONITOR, KMS 890+?
The FDA 510(k) record lists Keller Medical Specialties Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KELLER VITAL SIGNS MONITOR, KMS 890+?
The FDA product code for KELLER VITAL SIGNS MONITOR, KMS 890+ is DXN.
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 Keller Medical Specialties Products, 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: DXN)
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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