FDA 510(k)

HYCEL TRIGYCERIDE II TEST

K-Number: K802422 · 1980-10-06

Decision Date1980-10-06

Product Code

DecisionUnknown

Device Summary

HYCEL TRIGYCERIDE II TEST is the device name listed in this FDA 510(k) record. The listed applicant is Hycel, Inc.. It received FDA 510(k) clearance on 1980-10-06 under 510(k) number K802422. FDA Decision: Unknown.

Frequently Asked Questions

What is the HYCEL TRIGYCERIDE II TEST?

HYCEL TRIGYCERIDE II TEST is a medical device that received FDA 510(k) clearance on 1980-10-06. The listed applicant is Hycel, Inc.. The 510(k) number is K802422.

When did HYCEL TRIGYCERIDE II TEST receive FDA 510(k) clearance?

HYCEL TRIGYCERIDE II TEST received FDA 510(k) clearance on 1980-10-06, under 510(k) number K802422.

Who is the listed applicant for HYCEL TRIGYCERIDE II TEST?

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

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Other records listing Hycel, Inc. as applicant

K790335HYCEL M K782176HYCEL LDH-INT TEST K782116KETOSTEROID TEST, HYCEL-17 K782100HYCEL COUNTER 333 K782102HYCEL COUNTER 211 K782101HYCEL COUNTER 222

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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.