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FDA 510(k)

MULTI-AD FLUID DISPENSING PUMP MP-3000

K-Number: K801008 · 1980-06-02

Decision Date1980-06-02
Product CodeKYX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MULTI-AD FLUID DISPENSING PUMP MP-3000 is the device name listed in this FDA 510(k) record. The listed applicant is Burron Medical Products, Inc.. It received FDA 510(k) clearance on 1980-06-02 under 510(k) number K801008. The device is classified under product code KYX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTI-AD FLUID DISPENSING PUMP MP-3000?

MULTI-AD FLUID DISPENSING PUMP MP-3000 is a medical device that received FDA 510(k) clearance on 1980-06-02. The listed applicant is Burron Medical Products, Inc.. The 510(k) number is K801008.

When did MULTI-AD FLUID DISPENSING PUMP MP-3000 receive FDA 510(k) clearance?

MULTI-AD FLUID DISPENSING PUMP MP-3000 received FDA 510(k) clearance on 1980-06-02, under 510(k) number K801008.

Who is the listed applicant for MULTI-AD FLUID DISPENSING PUMP MP-3000?

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

What is the FDA product code for MULTI-AD FLUID DISPENSING PUMP MP-3000?

The FDA product code for MULTI-AD FLUID DISPENSING PUMP MP-3000 is KYX.

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 Burron Medical Products, 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 41 devices →

Related Devices (Code: KYX)

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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