OXYGENATORS #BOS-10, 105, 5S
K-Number: K823456 · 1982-12-30
Advertisement
Device Summary
Frequently Asked Questions
What is the OXYGENATORS #BOS-10, 105, 5S?
OXYGENATORS #BOS-10, 105, 5S is a medical device that received FDA 510(k) clearance on 1982-12-30. The listed applicant is Bentley Laboratories, Inc.. The 510(k) number is K823456.
When did OXYGENATORS #BOS-10, 105, 5S receive FDA 510(k) clearance?
OXYGENATORS #BOS-10, 105, 5S received FDA 510(k) clearance on 1982-12-30, under 510(k) number K823456.
Who is the listed applicant for OXYGENATORS #BOS-10, 105, 5S?
The FDA 510(k) record lists Bentley Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OXYGENATORS #BOS-10, 105, 5S?
The FDA product code for OXYGENATORS #BOS-10, 105, 5S is DTZ.
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 Bentley Laboratories, 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: DTZ)
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