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)

SOF-TOUCH NASAL CANNULA CAT.#304 & 305

K-Number: K802062 · 1980-09-09

ApplicantHospitak, Inc.
Decision Date1980-09-09
Product CodeCAT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SOF-TOUCH NASAL CANNULA CAT.#304 & 305 is the device name listed in this FDA 510(k) record. The listed applicant is Hospitak, Inc.. It received FDA 510(k) clearance on 1980-09-09 under 510(k) number K802062. The device is classified under product code CAT. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SOF-TOUCH NASAL CANNULA CAT.#304 & 305?

SOF-TOUCH NASAL CANNULA CAT.#304 & 305 is a medical device that received FDA 510(k) clearance on 1980-09-09. The listed applicant is Hospitak, Inc.. The 510(k) number is K802062.

When did SOF-TOUCH NASAL CANNULA CAT.#304 & 305 receive FDA 510(k) clearance?

SOF-TOUCH NASAL CANNULA CAT.#304 & 305 received FDA 510(k) clearance on 1980-09-09, under 510(k) number K802062.

Who is the listed applicant for SOF-TOUCH NASAL CANNULA CAT.#304 & 305?

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

What is the FDA product code for SOF-TOUCH NASAL CANNULA CAT.#304 & 305?

The FDA product code for SOF-TOUCH NASAL CANNULA CAT.#304 & 305 is CAT.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Hospitak, Inc. 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.

K955483TRACH MASK MODEL (245, 246)K954787ILLUMINATORK953620WARM N WET HMEF W/LUER ADAPTERK953619WARM N WET HME W/LUER ADAPTERK915750DISPOSABLE BACTERIAL BREATHNG FILTERK920842AEROSOL DELIVERY SYSTEMS

View all 27 devices →

Related Devices (Code: CAT)

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.

K011125NASAL CANNULA, WITH AND WITHOUT SUPPLY TUBING, AND OTHER SIMILAR NASAL CANNULA MANUFACTURED BY HRCIHudson Respiratory Care, Inc.K935533NASAL CANNULAPuritas Health Care, Inc.K9223974 SURE TM NASAL OXYGEN CANNULABoston Pacific Medical, Inc.K921496SKIN SAVER(TM) TUBING HOLDER, MODEL 1921 MODIFIEDAlpine Specialties, Inc.K920573CANNULA NASAL OXYGENB & F Medical Products, Inc.K913421NASAL OXYGEN CANNULA, 81585, 81587 & 81589Specialty Packaging Producs, Inc.

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.

↑