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FDA 510(k)

RADIAL IMMUNODIFFUSION PLATES

K-Number: K830911 · 1983-06-10

ApplicantBiocell Laboratories, Inc.
Decision Date1983-06-10
Product CodeDDG
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

RADIAL IMMUNODIFFUSION PLATES is the device name listed in this FDA 510(k) record. The listed applicant is Biocell Laboratories, Inc.. It received FDA 510(k) clearance on 1983-06-10 under 510(k) number K830911. The device is classified under product code DDG. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RADIAL IMMUNODIFFUSION PLATES?

RADIAL IMMUNODIFFUSION PLATES is a medical device that received FDA 510(k) clearance on 1983-06-10. The listed applicant is Biocell Laboratories, Inc.. The 510(k) number is K830911.

When did RADIAL IMMUNODIFFUSION PLATES receive FDA 510(k) clearance?

RADIAL IMMUNODIFFUSION PLATES received FDA 510(k) clearance on 1983-06-10, under 510(k) number K830911.

Who is the listed applicant for RADIAL IMMUNODIFFUSION PLATES?

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

What is the FDA product code for RADIAL IMMUNODIFFUSION PLATES?

The FDA product code for RADIAL IMMUNODIFFUSION PLATES is DDG.

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Other records listing Biocell Laboratories, Inc. as applicant

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Related Devices (Code: DDG)

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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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