ELI URINE CONTROLS
K-Number: K951817 · 1995-06-19
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Device Summary
Frequently Asked Questions
What is the ELI URINE CONTROLS?
ELI URINE CONTROLS is a medical device that received FDA 510(k) clearance on 1995-06-19. The listed applicant is Elsohly Labs, Inc.. The 510(k) number is K951817.
When did ELI URINE CONTROLS receive FDA 510(k) clearance?
ELI URINE CONTROLS received FDA 510(k) clearance on 1995-06-19, under 510(k) number K951817.
Who is the listed applicant for ELI URINE CONTROLS?
The FDA 510(k) record lists Elsohly Labs, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ELI URINE CONTROLS?
The FDA product code for ELI URINE CONTROLS is DIF.
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.
Related Devices (Code: DIF)
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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