Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

IMMUNOGL. FRACT. OF RABBIT ANTIS./LAMBDA

K-Number: K812662 · 1981-09-29

ApplicantDako Corp.
Decision Date1981-09-29
Product CodeDEH
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

IMMUNOGL. FRACT. OF RABBIT ANTIS./LAMBDA is the device name listed in this FDA 510(k) record. The listed applicant is Dako Corp.. It received FDA 510(k) clearance on 1981-09-29 under 510(k) number K812662. The device is classified under product code DEH. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMMUNOGL. FRACT. OF RABBIT ANTIS./LAMBDA?

IMMUNOGL. FRACT. OF RABBIT ANTIS./LAMBDA is a medical device that received FDA 510(k) clearance on 1981-09-29. The listed applicant is Dako Corp.. The 510(k) number is K812662.

When did IMMUNOGL. FRACT. OF RABBIT ANTIS./LAMBDA receive FDA 510(k) clearance?

IMMUNOGL. FRACT. OF RABBIT ANTIS./LAMBDA received FDA 510(k) clearance on 1981-09-29, under 510(k) number K812662.

Who is the listed applicant for IMMUNOGL. FRACT. OF RABBIT ANTIS./LAMBDA?

The FDA 510(k) record lists Dako Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IMMUNOGL. FRACT. OF RABBIT ANTIS./LAMBDA?

The FDA product code for IMMUNOGL. FRACT. OF RABBIT ANTIS./LAMBDA is DEH.

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 Dako 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.

View all 54 devices →

Related Devices (Code: DEH)

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.

↑