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FDA 510(k)

LAMB SERUM - STERILE FILTERED

K-Number: K861809 · 1986-05-20

Decision Date1986-05-20
Product CodeKIS
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

LAMB SERUM - STERILE FILTERED is the device name listed in this FDA 510(k) record. The listed applicant is Hazleton Research Products, Inc.. It received FDA 510(k) clearance on 1986-05-20 under 510(k) number K861809. The device is classified under product code KIS. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LAMB SERUM - STERILE FILTERED?

LAMB SERUM - STERILE FILTERED is a medical device that received FDA 510(k) clearance on 1986-05-20. The listed applicant is Hazleton Research Products, Inc.. The 510(k) number is K861809.

When did LAMB SERUM - STERILE FILTERED receive FDA 510(k) clearance?

LAMB SERUM - STERILE FILTERED received FDA 510(k) clearance on 1986-05-20, under 510(k) number K861809.

Who is the listed applicant for LAMB SERUM - STERILE FILTERED?

The FDA 510(k) record lists Hazleton Research Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LAMB SERUM - STERILE FILTERED?

The FDA product code for LAMB SERUM - STERILE FILTERED is KIS.

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 Hazleton Research Products, Inc. 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 47 devices →

Related Devices (Code: KIS)

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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