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FDA 510(k)

LACTALBUMIN HYDROLYSATE (ELAH) NO. L3762

K-Number: K870485 · 1987-03-30

Decision Date1987-03-30
Product CodeKIT
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

LACTALBUMIN HYDROLYSATE (ELAH) NO. L3762 is the device name listed in this FDA 510(k) record. The listed applicant is Sigma Chemical Co.. It received FDA 510(k) clearance on 1987-03-30 under 510(k) number K870485. The device is classified under product code KIT. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LACTALBUMIN HYDROLYSATE (ELAH) NO. L3762?

LACTALBUMIN HYDROLYSATE (ELAH) NO. L3762 is a medical device that received FDA 510(k) clearance on 1987-03-30. The listed applicant is Sigma Chemical Co.. The 510(k) number is K870485.

When did LACTALBUMIN HYDROLYSATE (ELAH) NO. L3762 receive FDA 510(k) clearance?

LACTALBUMIN HYDROLYSATE (ELAH) NO. L3762 received FDA 510(k) clearance on 1987-03-30, under 510(k) number K870485.

Who is the listed applicant for LACTALBUMIN HYDROLYSATE (ELAH) NO. L3762?

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 (ELAH) NO. L3762?

The FDA product code for LACTALBUMIN HYDROLYSATE (ELAH) NO. L3762 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.

View all 231 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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