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FDA 510(k)

TRYPIN (125I) RIA KIT

K-Number: K811805 · 1981-08-31

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1981-08-31
Product CodeJNO
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

TRYPIN (125I) RIA KIT 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 1981-08-31 under 510(k) number K811805. The device is classified under product code JNO. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRYPIN (125I) RIA KIT?

TRYPIN (125I) RIA KIT is a medical device that received FDA 510(k) clearance on 1981-08-31. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K811805.

When did TRYPIN (125I) RIA KIT receive FDA 510(k) clearance?

TRYPIN (125I) RIA KIT received FDA 510(k) clearance on 1981-08-31, under 510(k) number K811805.

Who is the listed applicant for TRYPIN (125I) RIA KIT?

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 TRYPIN (125I) RIA KIT?

The FDA product code for TRYPIN (125I) RIA KIT is JNO.

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Related Devices (Code: JNO)

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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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