SCORE SOFTWARE
K-Number: K961450 · 1996-08-01
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Device Summary
Frequently Asked Questions
What is the SCORE SOFTWARE?
SCORE SOFTWARE is a medical device that received FDA 510(k) clearance on 1996-08-01. The listed applicant is Nellcor Puritan Bennett, Inc.. The 510(k) number is K961450.
When did SCORE SOFTWARE receive FDA 510(k) clearance?
SCORE SOFTWARE received FDA 510(k) clearance on 1996-08-01, under 510(k) number K961450.
Who is the listed applicant for SCORE SOFTWARE?
The FDA 510(k) record lists Nellcor Puritan Bennett, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SCORE SOFTWARE?
The FDA product code for SCORE SOFTWARE 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 Nellcor Puritan Bennett, 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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