URINE SAMPLE KIT
K-Number: K780336 · 1978-04-03
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Device Summary
Frequently Asked Questions
What is the URINE SAMPLE KIT?
URINE SAMPLE KIT is a medical device that received FDA 510(k) clearance on 1978-04-03. The listed applicant is American Hospital Supply Corp.. The 510(k) number is K780336.
When did URINE SAMPLE KIT receive FDA 510(k) clearance?
URINE SAMPLE KIT received FDA 510(k) clearance on 1978-04-03, under 510(k) number K780336.
Who is the listed applicant for URINE SAMPLE KIT?
The FDA 510(k) record lists American Hospital Supply Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for URINE SAMPLE KIT?
The FDA product code for URINE SAMPLE KIT is KDD.
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 American Hospital Supply Corp. 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: KDD)
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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