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FDA 510(k)

HALL OSCILLATOR

K-Number: K832187 · 1983-08-12

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

Device Summary

HALL OSCILLATOR 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 K832187. 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 OSCILLATOR?

HALL OSCILLATOR 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 K832187.

When did HALL OSCILLATOR receive FDA 510(k) clearance?

HALL OSCILLATOR received FDA 510(k) clearance on 1983-08-12, under 510(k) number K832187.

Who is the listed applicant for HALL OSCILLATOR?

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 OSCILLATOR?

The FDA product code for HALL OSCILLATOR 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/AERAK832186HALL DRILL/REAMERK832188HALL RECIPROCATOR

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Related Devices (Code: GET)

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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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