FDA 510(k)

HALL ARTHROTOME

K-Number: K832816 · 1983-11-28

Decision Date1983-11-28

Product Code

DecisionSubstantially Equivalent

Device Summary

HALL ARTHROTOME is the device name listed in this FDA 510(k) record. The listed applicant is American Sterilizer Co.. It received FDA 510(k) clearance on 1983-11-28 under 510(k) number K832816. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HALL ARTHROTOME?

HALL ARTHROTOME is a medical device that received FDA 510(k) clearance on 1983-11-28. The listed applicant is American Sterilizer Co.. The 510(k) number is K832816.

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

HALL ARTHROTOME received FDA 510(k) clearance on 1983-11-28, under 510(k) number K832816.

Who is the listed applicant for HALL ARTHROTOME?

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

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 American Sterilizer Co. as applicant

K943288AMSCO SQ240 SURGICAL LIGHT K931872THE EAGLE 3017 100% ETHYLENE OXIDE STERILIZER K922485CHEMDI-VHP CHEMICAL INDICATOR K930493QUANTUM 3080 SURGICAL TABLE K905816ORTHOVISION TABLE K896674AMSCO QUANTUM LIGHT

View all 36 devices →

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.