BOS-2S, SPIRAFLO BUBBLE INFANT OXYGEN.
K-Number: K823273 · 1983-01-05
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Device Summary
Frequently Asked Questions
What is the BOS-2S, SPIRAFLO BUBBLE INFANT OXYGEN.?
BOS-2S, SPIRAFLO BUBBLE INFANT OXYGEN. is a medical device that received FDA 510(k) clearance on 1983-01-05. The listed applicant is Bentley Laboratories, Inc.. The 510(k) number is K823273.
When did BOS-2S, SPIRAFLO BUBBLE INFANT OXYGEN. receive FDA 510(k) clearance?
BOS-2S, SPIRAFLO BUBBLE INFANT OXYGEN. received FDA 510(k) clearance on 1983-01-05, under 510(k) number K823273.
Who is the listed applicant for BOS-2S, SPIRAFLO BUBBLE INFANT OXYGEN.?
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 BOS-2S, SPIRAFLO BUBBLE INFANT OXYGEN.?
The FDA product code for BOS-2S, SPIRAFLO BUBBLE INFANT OXYGEN. 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.
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