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FDA 510(k)

HALL DRILL/REAMER

K-Number: K832186 · 1983-08-12

ApplicantAmsco Co.
Decision Date1983-08-12
Product CodeGET
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HALL DRILL/REAMER is the device name listed in this FDA 510(k) record. The listed applicant is Amsco Co.. It received FDA 510(k) clearance on 1983-08-12 under 510(k) number K832186. The device is classified under product code GET. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HALL DRILL/REAMER?

HALL DRILL/REAMER is a medical device that received FDA 510(k) clearance on 1983-08-12. The listed applicant is Amsco Co.. The 510(k) number is K832186.

When did HALL DRILL/REAMER receive FDA 510(k) clearance?

HALL DRILL/REAMER received FDA 510(k) clearance on 1983-08-12, under 510(k) number K832186.

Who is the listed applicant for HALL DRILL/REAMER?

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

What is the FDA product code for HALL DRILL/REAMER?

The FDA product code for HALL DRILL/REAMER is GET.

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Other records listing Amsco Co. 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.

K912471EAGLE 3000 SDSK854922AMSCO POLARIS SLK833187HALL OSTEONK832945EAGLE 2000 STERILIZER SERIES GAS/AERAK832187HALL OSCILLATORK832188HALL RECIPROCATOR

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Related Devices (Code: GET)

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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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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