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FDA 510(k)

ANHYDRIC INCUBATORS, CULTURE INCUBATOR

K-Number: K831592 · 1983-06-16

Decision Date1983-06-16
Product CodeJTQ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

ANHYDRIC INCUBATORS, CULTURE INCUBATOR 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 1983-06-16 under 510(k) number K831592. The device is classified under product code JTQ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANHYDRIC INCUBATORS, CULTURE INCUBATOR?

ANHYDRIC INCUBATORS, CULTURE INCUBATOR is a medical device that received FDA 510(k) clearance on 1983-06-16. The listed applicant is Boekel Industries, Inc.. The 510(k) number is K831592.

When did ANHYDRIC INCUBATORS, CULTURE INCUBATOR receive FDA 510(k) clearance?

ANHYDRIC INCUBATORS, CULTURE INCUBATOR received FDA 510(k) clearance on 1983-06-16, under 510(k) number K831592.

Who is the listed applicant for ANHYDRIC INCUBATORS, CULTURE INCUBATOR?

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 ANHYDRIC INCUBATORS, CULTURE INCUBATOR?

The FDA product code for ANHYDRIC INCUBATORS, CULTURE INCUBATOR is JTQ.

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: JTQ)

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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