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FDA 510(k)

MICRO TARGETING DRIVE SYSTEM

K-Number: K011775 · 2001-08-30

ApplicantFHC, Inc.
Decision Date2001-08-30
Product CodeHAW
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MICRO TARGETING DRIVE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is FHC, Inc.. It received FDA 510(k) clearance on 2001-08-30 under 510(k) number K011775. The device is classified under product code HAW. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRO TARGETING DRIVE SYSTEM?

MICRO TARGETING DRIVE SYSTEM is a medical device that received FDA 510(k) clearance on 2001-08-30. The listed applicant is FHC, Inc.. The 510(k) number is K011775.

When did MICRO TARGETING DRIVE SYSTEM receive FDA 510(k) clearance?

MICRO TARGETING DRIVE SYSTEM received FDA 510(k) clearance on 2001-08-30, under 510(k) number K011775.

Who is the listed applicant for MICRO TARGETING DRIVE SYSTEM?

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

What is the FDA product code for MICRO TARGETING DRIVE SYSTEM?

The FDA product code for MICRO TARGETING DRIVE SYSTEM is HAW.

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Other records listing FHC, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: HAW)

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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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