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FDA 510(k)

LUNG DIFFUSION GAS MIXTURE

K-Number: K882817 · 1988-08-15

ApplicantSwisco, Inc.
Decision Date1988-08-15
Product CodeBYK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LUNG DIFFUSION GAS MIXTURE is the device name listed in this FDA 510(k) record. The listed applicant is Swisco, Inc.. It received FDA 510(k) clearance on 1988-08-15 under 510(k) number K882817. The device is classified under product code BYK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LUNG DIFFUSION GAS MIXTURE?

LUNG DIFFUSION GAS MIXTURE is a medical device that received FDA 510(k) clearance on 1988-08-15. The listed applicant is Swisco, Inc.. The 510(k) number is K882817.

When did LUNG DIFFUSION GAS MIXTURE receive FDA 510(k) clearance?

LUNG DIFFUSION GAS MIXTURE received FDA 510(k) clearance on 1988-08-15, under 510(k) number K882817.

Who is the listed applicant for LUNG DIFFUSION GAS MIXTURE?

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

What is the FDA product code for LUNG DIFFUSION GAS MIXTURE?

The FDA product code for LUNG DIFFUSION GAS MIXTURE is BYK.

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.

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Other records listing Swisco, 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.

K882941BLOOD GAS MIXTUREK882942LASER MIXTURE

Related Devices (Code: BYK)

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.

K941547CAM 4 THERMOELECTRIC CHILD/ADULT MIST TENTAllied Healthcare Products, Inc.K813235DISS FEMALE AIR ADAPTORTimeter Instrument Corp.

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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