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FDA 510(k)

ANESTHESIA VENTILATOR MODEL 100

K-Number: K854202 · 1986-04-11

ApplicantRusz Instruments, Inc.
Decision Date1986-04-11
Product CodeCAD
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ANESTHESIA VENTILATOR MODEL 100 is the device name listed in this FDA 510(k) record. The listed applicant is Rusz Instruments, Inc.. It received FDA 510(k) clearance on 1986-04-11 under 510(k) number K854202. The device is classified under product code CAD. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANESTHESIA VENTILATOR MODEL 100?

ANESTHESIA VENTILATOR MODEL 100 is a medical device that received FDA 510(k) clearance on 1986-04-11. The listed applicant is Rusz Instruments, Inc.. The 510(k) number is K854202.

When did ANESTHESIA VENTILATOR MODEL 100 receive FDA 510(k) clearance?

ANESTHESIA VENTILATOR MODEL 100 received FDA 510(k) clearance on 1986-04-11, under 510(k) number K854202.

Who is the listed applicant for ANESTHESIA VENTILATOR MODEL 100?

The FDA 510(k) record lists Rusz Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ANESTHESIA VENTILATOR MODEL 100?

The FDA product code for ANESTHESIA VENTILATOR MODEL 100 is CAD.

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Related Devices (Code: CAD)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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