OXICOM-2100
K-Number: K921519 · 1992-10-23
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Device Summary
Frequently Asked Questions
What is the OXICOM-2100?
OXICOM-2100 is a medical device that received FDA 510(k) clearance on 1992-10-23. The listed applicant is Waters Instruments, Inc.. The 510(k) number is K921519.
When did OXICOM-2100 receive FDA 510(k) clearance?
OXICOM-2100 received FDA 510(k) clearance on 1992-10-23, under 510(k) number K921519.
Who is the listed applicant for OXICOM-2100?
The FDA 510(k) record lists Waters Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OXICOM-2100?
The FDA product code for OXICOM-2100 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 Waters Instruments, 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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