HARRISON HAND HELD ADJUSTING INSTRUMENT
K-Number: K010851 · 2001-09-18
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Device Summary
Frequently Asked Questions
What is the HARRISON HAND HELD ADJUSTING INSTRUMENT?
HARRISON HAND HELD ADJUSTING INSTRUMENT is a medical device that received FDA 510(k) clearance on 2001-09-18. The listed applicant is Harrison Cbp Seminars. The 510(k) number is K010851.
When did HARRISON HAND HELD ADJUSTING INSTRUMENT receive FDA 510(k) clearance?
HARRISON HAND HELD ADJUSTING INSTRUMENT received FDA 510(k) clearance on 2001-09-18, under 510(k) number K010851.
Who is the listed applicant for HARRISON HAND HELD ADJUSTING INSTRUMENT?
The FDA 510(k) record lists Harrison Cbp Seminars as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HARRISON HAND HELD ADJUSTING INSTRUMENT?
The FDA product code for HARRISON HAND HELD ADJUSTING INSTRUMENT is LXM.
Related Clinical Trials
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.
Related Devices (Code: LXM)
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.
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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