MS-900S, MS-900SPM & MS-900SFM
K-Number: K980845 · 1998-12-14
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Device Summary
Frequently Asked Questions
What is the MS-900S, MS-900SPM & MS-900SFM?
MS-900S, MS-900SPM & MS-900SFM is a medical device that received FDA 510(k) clearance on 1998-12-14. The listed applicant is Mars Medical Products. The 510(k) number is K980845.
When did MS-900S, MS-900SPM & MS-900SFM receive FDA 510(k) clearance?
MS-900S, MS-900SPM & MS-900SFM received FDA 510(k) clearance on 1998-12-14, under 510(k) number K980845.
Who is the listed applicant for MS-900S, MS-900SPM & MS-900SFM?
The FDA 510(k) record lists Mars Medical Products as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MS-900S, MS-900SPM & MS-900SFM?
The FDA product code for MS-900S, MS-900SPM & MS-900SFM is DXN.
Other records listing Mars Medical Products 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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