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FDA 510(k)

BLOOD GAS INCUBATOR #260650

K-Number: K823766 · 1983-02-18

Decision Date1983-02-18
Product CodeJRG
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BLOOD GAS INCUBATOR #260650 is the device name listed in this FDA 510(k) record. The listed applicant is Boekel Industries, Inc.. It received FDA 510(k) clearance on 1983-02-18 under 510(k) number K823766. The device is classified under product code JRG. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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