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FDA 510(k)

NEEDLE BENDER TX8225

K-Number: K834108 · 1984-03-12

ApplicantToday'S Machining & Design, Inc.
Decision Date1984-03-12
Product CodeLXH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

NEEDLE BENDER TX8225 is the device name listed in this FDA 510(k) record. The listed applicant is Today'S Machining & Design, Inc.. It received FDA 510(k) clearance on 1984-03-12 under 510(k) number K834108. The device is classified under product code LXH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEEDLE BENDER TX8225?

NEEDLE BENDER TX8225 is a medical device that received FDA 510(k) clearance on 1984-03-12. The listed applicant is Today'S Machining & Design, Inc.. The 510(k) number is K834108.

When did NEEDLE BENDER TX8225 receive FDA 510(k) clearance?

NEEDLE BENDER TX8225 received FDA 510(k) clearance on 1984-03-12, under 510(k) number K834108.

Who is the listed applicant for NEEDLE BENDER TX8225?

The FDA 510(k) record lists Today'S Machining & Design, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEEDLE BENDER TX8225?

The FDA product code for NEEDLE BENDER TX8225 is LXH.

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.

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Other records listing Today'S Machining & Design, 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.

K853604ACE-KYLE DYE INJECTION NEEDLE P/N 14082K823676DISC NEEDLE SET #TX-8220K823675FRONING GUIDANCE SYSTEM #TX-8200

Related Devices (Code: LXH)

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.

K192873SX-One MicroKnifeSonex Health, Inc.K101609SELF RETAINING SOFT TISSUE RETRACTORKoros USA, Inc.K001507MICROPERFORATION INSTRUMENTSmith & Nephew, Inc.K952495ANCHORS AWAY SOFT TISSUE ATTACHMENT SYSTEMOrthopedic Systems, Inc.K943873ORTHOMET ANATOMICALLY GUIDED CARPAL TUNNEL RELEASE SYOrthomet, Inc.K944188SPINAL MARKERLeibinger L.P.

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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