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FDA 510(k)

AMBU UNIVERSAL SUCTION PUMP

K-Number: K792592 · 1980-01-11

Decision Date1980-01-11
Product CodeJCX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

AMBU UNIVERSAL SUCTION PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Narco Air-Shields. It received FDA 510(k) clearance on 1980-01-11 under 510(k) number K792592. The device is classified under product code JCX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMBU UNIVERSAL SUCTION PUMP?

AMBU UNIVERSAL SUCTION PUMP is a medical device that received FDA 510(k) clearance on 1980-01-11. The listed applicant is Narco Air-Shields. The 510(k) number is K792592.

When did AMBU UNIVERSAL SUCTION PUMP receive FDA 510(k) clearance?

AMBU UNIVERSAL SUCTION PUMP received FDA 510(k) clearance on 1980-01-11, under 510(k) number K792592.

Who is the listed applicant for AMBU UNIVERSAL SUCTION PUMP?

The FDA 510(k) record lists Narco Air-Shields as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AMBU UNIVERSAL SUCTION PUMP?

The FDA product code for AMBU UNIVERSAL SUCTION PUMP is JCX.

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 Narco Air-Shields 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 19 devices →

Related Devices (Code: JCX)

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

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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