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FDA 510(k)

DISPOSABLE CO2 ABSORBER/E

K-Number: K897171 · 1990-03-13

ApplicantGibeck, Inc.
Decision Date1990-03-13
Product CodeCBL
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE CO2 ABSORBER/E is the device name listed in this FDA 510(k) record. The listed applicant is Gibeck, Inc.. It received FDA 510(k) clearance on 1990-03-13 under 510(k) number K897171. The device is classified under product code CBL. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE CO2 ABSORBER/E?

DISPOSABLE CO2 ABSORBER/E is a medical device that received FDA 510(k) clearance on 1990-03-13. The listed applicant is Gibeck, Inc.. The 510(k) number is K897171.

When did DISPOSABLE CO2 ABSORBER/E receive FDA 510(k) clearance?

DISPOSABLE CO2 ABSORBER/E received FDA 510(k) clearance on 1990-03-13, under 510(k) number K897171.

Who is the listed applicant for DISPOSABLE CO2 ABSORBER/E?

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

What is the FDA product code for DISPOSABLE CO2 ABSORBER/E?

The FDA product code for DISPOSABLE CO2 ABSORBER/E is CBL.

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 Gibeck, 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 15 devices →

Related Devices (Code: CBL)

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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