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FDA 510(k)

HYCOR ACCUPINCH THC TEST

K-Number: K901334 · 1990-05-14

ApplicantHycor Biomedical, Inc.
Decision Date1990-05-14
Product CodeLDJ
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

HYCOR ACCUPINCH THC TEST is the device name listed in this FDA 510(k) record. The listed applicant is Hycor Biomedical, Inc.. It received FDA 510(k) clearance on 1990-05-14 under 510(k) number K901334. The device is classified under product code LDJ. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HYCOR ACCUPINCH THC TEST?

HYCOR ACCUPINCH THC TEST is a medical device that received FDA 510(k) clearance on 1990-05-14. The listed applicant is Hycor Biomedical, Inc.. The 510(k) number is K901334.

When did HYCOR ACCUPINCH THC TEST receive FDA 510(k) clearance?

HYCOR ACCUPINCH THC TEST received FDA 510(k) clearance on 1990-05-14, under 510(k) number K901334.

Who is the listed applicant for HYCOR ACCUPINCH THC TEST?

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

What is the FDA product code for HYCOR ACCUPINCH THC TEST?

The FDA product code for HYCOR ACCUPINCH THC TEST is LDJ.

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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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