MODEL 8500 HAND HELD PULSE OXIMETER
K-Number: K893221 · 1990-02-28
Advertisement
Device Summary
Frequently Asked Questions
What is the MODEL 8500 HAND HELD PULSE OXIMETER?
MODEL 8500 HAND HELD PULSE OXIMETER is a medical device that received FDA 510(k) clearance on 1990-02-28. The listed applicant is Nonin Medical, Inc.. The 510(k) number is K893221.
When did MODEL 8500 HAND HELD PULSE OXIMETER receive FDA 510(k) clearance?
MODEL 8500 HAND HELD PULSE OXIMETER received FDA 510(k) clearance on 1990-02-28, under 510(k) number K893221.
Who is the listed applicant for MODEL 8500 HAND HELD PULSE OXIMETER?
The FDA 510(k) record lists Nonin Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODEL 8500 HAND HELD PULSE OXIMETER?
The FDA product code for MODEL 8500 HAND HELD PULSE OXIMETER 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 Nonin Medical, 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.
Advertisement