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FDA 510(k)

WARMAIR SYSTEM

K-Number: K910327 · 1991-05-16

Decision Date1991-05-16
Product CodeDWJ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

WARMAIR SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Cincinnati Sub-Zero Products, Inc.. It received FDA 510(k) clearance on 1991-05-16 under 510(k) number K910327. The device is classified under product code DWJ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WARMAIR SYSTEM?

WARMAIR SYSTEM is a medical device that received FDA 510(k) clearance on 1991-05-16. The listed applicant is Cincinnati Sub-Zero Products, Inc.. The 510(k) number is K910327.

When did WARMAIR SYSTEM receive FDA 510(k) clearance?

WARMAIR SYSTEM received FDA 510(k) clearance on 1991-05-16, under 510(k) number K910327.

Who is the listed applicant for WARMAIR SYSTEM?

The FDA 510(k) record lists Cincinnati Sub-Zero Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WARMAIR SYSTEM?

The FDA product code for WARMAIR SYSTEM is DWJ.

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 Cincinnati Sub-Zero Products, 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.

View all 12 devices →

Related Devices (Code: DWJ)

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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