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FDA 510(k)

HYCOR ACCUPINCH MORPHINE TEST

K-Number: K900173 · 1990-03-30

ApplicantHycor Biomedical, Inc.
Decision Date1990-03-30
Product CodeDJG
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

HYCOR ACCUPINCH MORPHINE 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 1990-03-30 under 510(k) number K900173. The device is classified under product code DJG. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HYCOR ACCUPINCH MORPHINE TEST?

HYCOR ACCUPINCH MORPHINE TEST is a medical device that received FDA 510(k) clearance on 1990-03-30. The listed applicant is Hycor Biomedical, Inc.. The 510(k) number is K900173.

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

HYCOR ACCUPINCH MORPHINE TEST received FDA 510(k) clearance on 1990-03-30, under 510(k) number K900173.

Who is the listed applicant for HYCOR ACCUPINCH MORPHINE 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 MORPHINE TEST?

The FDA product code for HYCOR ACCUPINCH MORPHINE TEST is DJG.

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Other records listing Hycor Biomedical, Inc. as applicant

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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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