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FDA 510(k)

DEMISTIFIER ISOLATION CHAMBER

K-Number: K902161 · 1990-10-15

Decision Date1990-10-15
Product CodeCBN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DEMISTIFIER ISOLATION CHAMBER is the device name listed in this FDA 510(k) record. The listed applicant is Peace Medical, Inc.. It received FDA 510(k) clearance on 1990-10-15 under 510(k) number K902161. The device is classified under product code CBN. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEMISTIFIER ISOLATION CHAMBER?

DEMISTIFIER ISOLATION CHAMBER is a medical device that received FDA 510(k) clearance on 1990-10-15. The listed applicant is Peace Medical, Inc.. The 510(k) number is K902161.

When did DEMISTIFIER ISOLATION CHAMBER receive FDA 510(k) clearance?

DEMISTIFIER ISOLATION CHAMBER received FDA 510(k) clearance on 1990-10-15, under 510(k) number K902161.

Who is the listed applicant for DEMISTIFIER ISOLATION CHAMBER?

The FDA 510(k) record lists Peace Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DEMISTIFIER ISOLATION CHAMBER?

The FDA product code for DEMISTIFIER ISOLATION CHAMBER is CBN.

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 Peace Medical, 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: CBN)

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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