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FDA 510(k)

HOLOGIC MODEL WHF-1 ANTHROPOMORPHIC FEMUR PHANTOM

K-Number: K883360 · 1988-09-27

ApplicantHologic, Inc.
Decision Date1988-09-27
Product CodeKGI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

HOLOGIC MODEL WHF-1 ANTHROPOMORPHIC FEMUR PHANTOM is the device name listed in this FDA 510(k) record. The listed applicant is Hologic, Inc.. It received FDA 510(k) clearance on 1988-09-27 under 510(k) number K883360. The device is classified under product code KGI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HOLOGIC MODEL WHF-1 ANTHROPOMORPHIC FEMUR PHANTOM?

HOLOGIC MODEL WHF-1 ANTHROPOMORPHIC FEMUR PHANTOM is a medical device that received FDA 510(k) clearance on 1988-09-27. The listed applicant is Hologic, Inc.. The 510(k) number is K883360.

When did HOLOGIC MODEL WHF-1 ANTHROPOMORPHIC FEMUR PHANTOM receive FDA 510(k) clearance?

HOLOGIC MODEL WHF-1 ANTHROPOMORPHIC FEMUR PHANTOM received FDA 510(k) clearance on 1988-09-27, under 510(k) number K883360.

Who is the listed applicant for HOLOGIC MODEL WHF-1 ANTHROPOMORPHIC FEMUR PHANTOM?

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

What is the FDA product code for HOLOGIC MODEL WHF-1 ANTHROPOMORPHIC FEMUR PHANTOM?

The FDA product code for HOLOGIC MODEL WHF-1 ANTHROPOMORPHIC FEMUR PHANTOM is KGI.

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Other records listing Hologic, Inc. as applicant

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Related Devices (Code: KGI)

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.

K254072BoneVueCurvebeam AI / Curvebeam, LLCK252718Lunar AstraGE Medical Systems Ultrasound & Primary Care Diagnostics, LLCK2510223D-SHAPER3D-Shaper Medical S.LK242295BunkerHill BMDBunkerHill HealthK243218TBS iNsight (V4)Medimaps Group SAK220402VirtuOstO.N. Diagnostics

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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