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FDA 510(k)

MODULUS II ANESTHESIA GAS MACHINE

K-Number: K833335 · 1983-11-14

Decision Date1983-11-14
Product CodeBSZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MODULUS II ANESTHESIA GAS MACHINE is the device name listed in this FDA 510(k) record. The listed applicant is Ohio Medical Products. It received FDA 510(k) clearance on 1983-11-14 under 510(k) number K833335. The device is classified under product code BSZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODULUS II ANESTHESIA GAS MACHINE?

MODULUS II ANESTHESIA GAS MACHINE is a medical device that received FDA 510(k) clearance on 1983-11-14. The listed applicant is Ohio Medical Products. The 510(k) number is K833335.

When did MODULUS II ANESTHESIA GAS MACHINE receive FDA 510(k) clearance?

MODULUS II ANESTHESIA GAS MACHINE received FDA 510(k) clearance on 1983-11-14, under 510(k) number K833335.

Who is the listed applicant for MODULUS II ANESTHESIA GAS MACHINE?

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

What is the FDA product code for MODULUS II ANESTHESIA GAS MACHINE?

The FDA product code for MODULUS II ANESTHESIA GAS MACHINE is BSZ.

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.

Other records listing Ohio Medical Products 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.

View all 47 devices →

Related Devices (Code: BSZ)

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.

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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