9303 NEONATAL/ADULT VITAL SIGNS MONITOR
K-Number: K982776 · 1998-11-02
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Device Summary
Frequently Asked Questions
What is the 9303 NEONATAL/ADULT VITAL SIGNS MONITOR?
9303 NEONATAL/ADULT VITAL SIGNS MONITOR is a medical device that received FDA 510(k) clearance on 1998-11-02. The listed applicant is Cas Medical Systems, Inc.. The 510(k) number is K982776.
When did 9303 NEONATAL/ADULT VITAL SIGNS MONITOR receive FDA 510(k) clearance?
9303 NEONATAL/ADULT VITAL SIGNS MONITOR received FDA 510(k) clearance on 1998-11-02, under 510(k) number K982776.
Who is the listed applicant for 9303 NEONATAL/ADULT VITAL SIGNS MONITOR?
The FDA 510(k) record lists Cas Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 9303 NEONATAL/ADULT VITAL SIGNS MONITOR?
The FDA product code for 9303 NEONATAL/ADULT VITAL SIGNS MONITOR is DQA.
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 Cas Medical Systems, 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: DQA)
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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