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)

OEM MEDICAL ADULT ANESTHESIA BREATHING CIRCUIT

K-Number: K925893 · 1993-03-12

ApplicantOem Medical Div.
Decision Date1993-03-12
Product CodeCAI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

OEM MEDICAL ADULT ANESTHESIA BREATHING CIRCUIT is the device name listed in this FDA 510(k) record. The listed applicant is Oem Medical Div.. It received FDA 510(k) clearance on 1993-03-12 under 510(k) number K925893. The device is classified under product code CAI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OEM MEDICAL ADULT ANESTHESIA BREATHING CIRCUIT?

OEM MEDICAL ADULT ANESTHESIA BREATHING CIRCUIT is a medical device that received FDA 510(k) clearance on 1993-03-12. The listed applicant is Oem Medical Div.. The 510(k) number is K925893.

When did OEM MEDICAL ADULT ANESTHESIA BREATHING CIRCUIT receive FDA 510(k) clearance?

OEM MEDICAL ADULT ANESTHESIA BREATHING CIRCUIT received FDA 510(k) clearance on 1993-03-12, under 510(k) number K925893.

Who is the listed applicant for OEM MEDICAL ADULT ANESTHESIA BREATHING CIRCUIT?

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

What is the FDA product code for OEM MEDICAL ADULT ANESTHESIA BREATHING CIRCUIT?

The FDA product code for OEM MEDICAL ADULT ANESTHESIA BREATHING CIRCUIT is CAI.

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 Oem Medical Div. 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.

K924570OEM MULTI-VAC POWERED SUCTION PUMPK922748GUEDEL AIRWAYK811855SKIN SCRUB KITSK761297MOUTHPIECE SEAL

Related Devices (Code: CAI)

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.

K954480CONDENSATE COLLECTION KITNova-VentrxK953787UNICOR, INC. ADULT ANESTHESIA BREATHING CIRCUITUnicor, Inc.K953788UNICOR, INC. GAS SAMPLING LINES & CONNECTORSUnicor, Inc.K952016PRIMA PEDIATRIC GAS SAMPLING CIRCUITSPrima, Inc.K952018PRIMA COAXIAL CIRCUITSPrima, Inc.K952020PRIMA PEDIATRIC ANESTHESIA CIRCUITSPrima, 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.

↑