Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

OHIO CAL-CHEK

K-Number: K810290 · 1981-02-12

ApplicantOhio Medical Products
Decision Date1981-02-12
Product CodeBXW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

OHIO CAL-CHEK 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 1981-02-12 under 510(k) number K810290. The device is classified under product code BXW. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OHIO CAL-CHEK?

OHIO CAL-CHEK is a medical device that received FDA 510(k) clearance on 1981-02-12. The listed applicant is Ohio Medical Products. The 510(k) number is K810290.

When did OHIO CAL-CHEK receive FDA 510(k) clearance?

OHIO CAL-CHEK received FDA 510(k) clearance on 1981-02-12, under 510(k) number K810290.

Who is the listed applicant for OHIO CAL-CHEK?

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 OHIO CAL-CHEK?

The FDA product code for OHIO CAL-CHEK is BXW.

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

View all 47 devices →

Related Devices (Code: BXW)

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.

K853848RESPIRATORY DIAGNOSTIC EQUIPMENT CALIBRATORMedical Graphics Corp.K831758FLOW-CALIBRATION MODULEThe Perkin-Elmer Corp.K830898SYRINGE 500BC BE #7000Instrumentation Industries, Inc.K812765DATASCRIBE #DS-40Timeter Instrument Corp.K760520CALIPERS, MCGAW SKINFOLDMcgaw Laboratories

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.

↑