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FDA 510(k)

C.C.-PAK

K-Number: K800635 · 1980-04-10

ApplicantRespiratory Care, Inc.
Decision Date1980-04-10
Product CodeJOL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

C.C.-PAK is the device name listed in this FDA 510(k) record. The listed applicant is Respiratory Care, Inc.. It received FDA 510(k) clearance on 1980-04-10 under 510(k) number K800635. The device is classified under product code JOL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the C.C.-PAK?

C.C.-PAK is a medical device that received FDA 510(k) clearance on 1980-04-10. The listed applicant is Respiratory Care, Inc.. The 510(k) number is K800635.

When did C.C.-PAK receive FDA 510(k) clearance?

C.C.-PAK received FDA 510(k) clearance on 1980-04-10, under 510(k) number K800635.

Who is the listed applicant for C.C.-PAK?

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

What is the FDA product code for C.C.-PAK?

The FDA product code for C.C.-PAK is JOL.

Other records listing Respiratory Care, 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.

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Related Devices (Code: JOL)

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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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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