KONTRON PULSE OXIMETER 7840
K-Number: K890299 · 1989-03-02
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Device Summary
Frequently Asked Questions
What is the KONTRON PULSE OXIMETER 7840?
KONTRON PULSE OXIMETER 7840 is a medical device that received FDA 510(k) clearance on 1989-03-02. The listed applicant is Kontron Instruments, Inc.. The 510(k) number is K890299.
When did KONTRON PULSE OXIMETER 7840 receive FDA 510(k) clearance?
KONTRON PULSE OXIMETER 7840 received FDA 510(k) clearance on 1989-03-02, under 510(k) number K890299.
Who is the listed applicant for KONTRON PULSE OXIMETER 7840?
The FDA 510(k) record lists Kontron Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KONTRON PULSE OXIMETER 7840?
The FDA product code for KONTRON PULSE OXIMETER 7840 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 Kontron 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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