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FDA 510(k)

NEUMOVENT 980

K-Number: K821792 · 1982-08-02

ApplicantUltramar Marketing Corp.
Decision Date1982-08-02
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

NEUMOVENT 980 is the device name listed in this FDA 510(k) record. The listed applicant is Ultramar Marketing Corp.. It received FDA 510(k) clearance on 1982-08-02 under 510(k) number K821792. The device is classified under product code CBK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEUMOVENT 980?

NEUMOVENT 980 is a medical device that received FDA 510(k) clearance on 1982-08-02. The listed applicant is Ultramar Marketing Corp.. The 510(k) number is K821792.

When did NEUMOVENT 980 receive FDA 510(k) clearance?

NEUMOVENT 980 received FDA 510(k) clearance on 1982-08-02, under 510(k) number K821792.

Who is the listed applicant for NEUMOVENT 980?

The FDA 510(k) record lists Ultramar Marketing Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEUMOVENT 980?

The FDA product code for NEUMOVENT 980 is CBK.

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Related Devices (Code: CBK)

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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