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FDA 510(k)

SICKLE-2000

K-Number: K955719 · 1996-08-14

ApplicantMedicus Technologies, Inc.
Decision Date1996-08-14
Product CodeGIQ
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

SICKLE-2000 is the device name listed in this FDA 510(k) record. The listed applicant is Medicus Technologies, Inc.. It received FDA 510(k) clearance on 1996-08-14 under 510(k) number K955719. The device is classified under product code GIQ. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SICKLE-2000?

SICKLE-2000 is a medical device that received FDA 510(k) clearance on 1996-08-14. The listed applicant is Medicus Technologies, Inc.. The 510(k) number is K955719.

When did SICKLE-2000 receive FDA 510(k) clearance?

SICKLE-2000 received FDA 510(k) clearance on 1996-08-14, under 510(k) number K955719.

Who is the listed applicant for SICKLE-2000?

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

What is the FDA product code for SICKLE-2000?

The FDA product code for SICKLE-2000 is GIQ.

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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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