FLEXIFLO COMPANION ENTERAL NUTRITION PUMP
K-Number: K873119 · 1987-11-05
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Device Summary
Frequently Asked Questions
What is the FLEXIFLO COMPANION ENTERAL NUTRITION PUMP?
FLEXIFLO COMPANION ENTERAL NUTRITION PUMP is a medical device that received FDA 510(k) clearance on 1987-11-05. The listed applicant is Frantz Medical Development, Ltd.. The 510(k) number is K873119.
When did FLEXIFLO COMPANION ENTERAL NUTRITION PUMP receive FDA 510(k) clearance?
FLEXIFLO COMPANION ENTERAL NUTRITION PUMP received FDA 510(k) clearance on 1987-11-05, under 510(k) number K873119.
Who is the listed applicant for FLEXIFLO COMPANION ENTERAL NUTRITION PUMP?
The FDA 510(k) record lists Frantz Medical Development, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FLEXIFLO COMPANION ENTERAL NUTRITION PUMP?
The FDA product code for FLEXIFLO COMPANION ENTERAL NUTRITION PUMP is LZH.
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 Frantz Medical Development, Ltd. 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: LZH)
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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