LACTALBUMIN HYDROLYSATE MED. CATALOG
K-Number: K843045 · 1984-08-12
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Device Summary
Frequently Asked Questions
What is the LACTALBUMIN HYDROLYSATE MED. CATALOG?
LACTALBUMIN HYDROLYSATE MED. CATALOG is a medical device that received FDA 510(k) clearance on 1984-08-12. The listed applicant is Sigma Chemical Co.. The 510(k) number is K843045.
When did LACTALBUMIN HYDROLYSATE MED. CATALOG receive FDA 510(k) clearance?
LACTALBUMIN HYDROLYSATE MED. CATALOG received FDA 510(k) clearance on 1984-08-12, under 510(k) number K843045.
Who is the listed applicant for LACTALBUMIN HYDROLYSATE MED. CATALOG?
The FDA 510(k) record lists Sigma Chemical Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LACTALBUMIN HYDROLYSATE MED. CATALOG?
The FDA product code for LACTALBUMIN HYDROLYSATE MED. CATALOG is KIT.
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 Sigma Chemical Co. 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: KIT)
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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