MULTI-AD FLUID DISPENSING PUMP MP-3000
K-Number: K801008 · 1980-06-02
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Device Summary
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.
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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