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FDA 510(k)

ANTIBODY TO INTRINSIC FACTOR RADIOASSAY

K-Number: K833142 · 1984-01-30

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1984-01-30
Product CodeCDD
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ANTIBODY TO INTRINSIC FACTOR RADIOASSAY is the device name listed in this FDA 510(k) record. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. It received FDA 510(k) clearance on 1984-01-30 under 510(k) number K833142. The device is classified under product code CDD. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANTIBODY TO INTRINSIC FACTOR RADIOASSAY?

ANTIBODY TO INTRINSIC FACTOR RADIOASSAY is a medical device that received FDA 510(k) clearance on 1984-01-30. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K833142.

When did ANTIBODY TO INTRINSIC FACTOR RADIOASSAY receive FDA 510(k) clearance?

ANTIBODY TO INTRINSIC FACTOR RADIOASSAY received FDA 510(k) clearance on 1984-01-30, under 510(k) number K833142.

Who is the listed applicant for ANTIBODY TO INTRINSIC FACTOR RADIOASSAY?

The FDA 510(k) record lists Bd Becton Dickinson Vacutainer Systems Preanalytic as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ANTIBODY TO INTRINSIC FACTOR RADIOASSAY?

The FDA product code for ANTIBODY TO INTRINSIC FACTOR RADIOASSAY is CDD.

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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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