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FDA 510(k)

OXYGEN & RESUSCITATION (HOPE II MODEL)

K-Number: K760101 · 1976-07-15

ApplicantOhio Medical Products
Decision Date1976-07-15
Product Code
DecisionSubstantially Equivalent

Device Summary

OXYGEN & RESUSCITATION (HOPE II MODEL) 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 1976-07-15 under 510(k) number K760101. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OXYGEN & RESUSCITATION (HOPE II MODEL)?

OXYGEN & RESUSCITATION (HOPE II MODEL) is a medical device that received FDA 510(k) clearance on 1976-07-15. The listed applicant is Ohio Medical Products. The 510(k) number is K760101.

When did OXYGEN & RESUSCITATION (HOPE II MODEL) receive FDA 510(k) clearance?

OXYGEN & RESUSCITATION (HOPE II MODEL) received FDA 510(k) clearance on 1976-07-15, under 510(k) number K760101.

Who is the listed applicant for OXYGEN & RESUSCITATION (HOPE II MODEL)?

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

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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.

K841733OHIO WASTE GAS SCAVENGING RESERVOIRK842003OHIO WASTE GAS SCAVENGING INTERFACEK840356OHIO UNITROL II ANESTHESIA GAS MACHINEK841274BAG-TO-VENTILATOR SELECTOR VALVEK840967OHIO HEAT REFLECTING PATCHK840857OHIO 3000 INFANT WARMER SYSTEM

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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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