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FDA 510(k)

CRYPTO-CEL IF TEST

K-Number: K955852 · 1996-08-05

ApplicantTechlab, Inc.
Decision Date1996-08-05
Product CodeMHJ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CRYPTO-CEL IF TEST is the device name listed in this FDA 510(k) record. The listed applicant is Techlab, Inc.. It received FDA 510(k) clearance on 1996-08-05 under 510(k) number K955852. The device is classified under product code MHJ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CRYPTO-CEL IF TEST?

CRYPTO-CEL IF TEST is a medical device that received FDA 510(k) clearance on 1996-08-05. The listed applicant is Techlab, Inc.. The 510(k) number is K955852.

When did CRYPTO-CEL IF TEST receive FDA 510(k) clearance?

CRYPTO-CEL IF TEST received FDA 510(k) clearance on 1996-08-05, under 510(k) number K955852.

Who is the listed applicant for CRYPTO-CEL IF TEST?

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

What is the FDA product code for CRYPTO-CEL IF TEST?

The FDA product code for CRYPTO-CEL IF TEST is MHJ.

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Related Devices (Code: MHJ)

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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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