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FDA 510(k)

DAKO MOUSE ANTI-HUMAN B-CELL (DAKO-C020-L26 MONO ANTI

K-Number: K924726 · 1994-06-13

ApplicantDako Corp.
Decision Date1994-06-13
Product CodeDEH
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

DAKO MOUSE ANTI-HUMAN B-CELL (DAKO-C020-L26 MONO ANTI is the device name listed in this FDA 510(k) record. The listed applicant is Dako Corp.. It received FDA 510(k) clearance on 1994-06-13 under 510(k) number K924726. 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 DAKO MOUSE ANTI-HUMAN B-CELL (DAKO-C020-L26 MONO ANTI?

DAKO MOUSE ANTI-HUMAN B-CELL (DAKO-C020-L26 MONO ANTI is a medical device that received FDA 510(k) clearance on 1994-06-13. The listed applicant is Dako Corp.. The 510(k) number is K924726.

When did DAKO MOUSE ANTI-HUMAN B-CELL (DAKO-C020-L26 MONO ANTI receive FDA 510(k) clearance?

DAKO MOUSE ANTI-HUMAN B-CELL (DAKO-C020-L26 MONO ANTI received FDA 510(k) clearance on 1994-06-13, under 510(k) number K924726.

Who is the listed applicant for DAKO MOUSE ANTI-HUMAN B-CELL (DAKO-C020-L26 MONO ANTI?

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 DAKO MOUSE ANTI-HUMAN B-CELL (DAKO-C020-L26 MONO ANTI?

The FDA product code for DAKO MOUSE ANTI-HUMAN B-CELL (DAKO-C020-L26 MONO ANTI 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.

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