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FDA 510(k)

ARTHROSCOPY FLUID MGMT. SYSTEM

K-Number: K832315 · 1983-10-04

Applicant3M Health Care, Sarns
Decision Date1983-10-04
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ARTHROSCOPY FLUID MGMT. SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is 3M Health Care, Sarns. It received FDA 510(k) clearance on 1983-10-04 under 510(k) number K832315. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTHROSCOPY FLUID MGMT. SYSTEM?

ARTHROSCOPY FLUID MGMT. SYSTEM is a medical device that received FDA 510(k) clearance on 1983-10-04. The listed applicant is 3M Health Care, Sarns. The 510(k) number is K832315.

When did ARTHROSCOPY FLUID MGMT. SYSTEM receive FDA 510(k) clearance?

ARTHROSCOPY FLUID MGMT. SYSTEM received FDA 510(k) clearance on 1983-10-04, under 510(k) number K832315.

Who is the listed applicant for ARTHROSCOPY FLUID MGMT. SYSTEM?

The FDA 510(k) record lists 3M Health Care, Sarns as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ARTHROSCOPY FLUID MGMT. SYSTEM?

The FDA product code for ARTHROSCOPY FLUID MGMT. SYSTEM is HRX.

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Related Devices (Code: HRX)

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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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