BLOOD GAS INCUBATOR #260650
K-Number: K823766 · 1983-02-18
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Device Summary
Frequently Asked Questions
What is the BLOOD GAS INCUBATOR #260650?
BLOOD GAS INCUBATOR #260650 is a medical device that received FDA 510(k) clearance on 1983-02-18. The listed applicant is Boekel Industries, Inc.. The 510(k) number is K823766.
When did BLOOD GAS INCUBATOR #260650 receive FDA 510(k) clearance?
BLOOD GAS INCUBATOR #260650 received FDA 510(k) clearance on 1983-02-18, under 510(k) number K823766.
Who is the listed applicant for BLOOD GAS INCUBATOR #260650?
The FDA 510(k) record lists Boekel Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BLOOD GAS INCUBATOR #260650?
The FDA product code for BLOOD GAS INCUBATOR #260650 is JRG.
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 Boekel Industries, 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: JRG)
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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