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FDA 510(k)

Y-TYPE BACKCHECK MICROBORE EXTEN. SET

K-Number: K831203 · 1983-06-03

ApplicantAbbott Laboratories
Decision Date1983-06-03
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Y-TYPE BACKCHECK MICROBORE EXTEN. SET is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1983-06-03 under 510(k) number K831203. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Y-TYPE BACKCHECK MICROBORE EXTEN. SET?

Y-TYPE BACKCHECK MICROBORE EXTEN. SET is a medical device that received FDA 510(k) clearance on 1983-06-03. The listed applicant is Abbott Laboratories. The 510(k) number is K831203.

When did Y-TYPE BACKCHECK MICROBORE EXTEN. SET receive FDA 510(k) clearance?

Y-TYPE BACKCHECK MICROBORE EXTEN. SET received FDA 510(k) clearance on 1983-06-03, under 510(k) number K831203.

Who is the listed applicant for Y-TYPE BACKCHECK MICROBORE EXTEN. SET?

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

What is the FDA product code for Y-TYPE BACKCHECK MICROBORE EXTEN. SET?

The FDA product code for Y-TYPE BACKCHECK MICROBORE EXTEN. SET is FRN.

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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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