GENTAMICIN LIQUID CONTROL SERUM
K-Number: K792262 · 1979-12-18
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Device Summary
Frequently Asked Questions
What is the GENTAMICIN LIQUID CONTROL SERUM?
GENTAMICIN LIQUID CONTROL SERUM is a medical device that received FDA 510(k) clearance on 1979-12-18. The listed applicant is Hemometrix. The 510(k) number is K792262.
When did GENTAMICIN LIQUID CONTROL SERUM receive FDA 510(k) clearance?
GENTAMICIN LIQUID CONTROL SERUM received FDA 510(k) clearance on 1979-12-18, under 510(k) number K792262.
Who is the listed applicant for GENTAMICIN LIQUID CONTROL SERUM?
The FDA 510(k) record lists Hemometrix as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GENTAMICIN LIQUID CONTROL SERUM?
The FDA product code for GENTAMICIN LIQUID CONTROL SERUM is LAS.
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 Hemometrix 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: LAS)
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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