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)

MERIDIAN MEDICAL SYSTEMS ADULT ANES BREATH CIRCUIT

K-Number: K925232 · 1993-01-22

ApplicantMerit Medical Systems, Inc.
Decision Date1993-01-22
Product CodeCAI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MERIDIAN MEDICAL SYSTEMS ADULT ANES BREATH CIRCUIT is the device name listed in this FDA 510(k) record. The listed applicant is Merit Medical Systems, Inc.. It received FDA 510(k) clearance on 1993-01-22 under 510(k) number K925232. 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 MERIDIAN MEDICAL SYSTEMS ADULT ANES BREATH CIRCUIT?

MERIDIAN MEDICAL SYSTEMS ADULT ANES BREATH CIRCUIT is a medical device that received FDA 510(k) clearance on 1993-01-22. The listed applicant is Merit Medical Systems, Inc.. The 510(k) number is K925232.

When did MERIDIAN MEDICAL SYSTEMS ADULT ANES BREATH CIRCUIT receive FDA 510(k) clearance?

MERIDIAN MEDICAL SYSTEMS ADULT ANES BREATH CIRCUIT received FDA 510(k) clearance on 1993-01-22, under 510(k) number K925232.

Who is the listed applicant for MERIDIAN MEDICAL SYSTEMS ADULT ANES BREATH CIRCUIT?

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

What is the FDA product code for MERIDIAN MEDICAL SYSTEMS ADULT ANES BREATH CIRCUIT?

The FDA product code for MERIDIAN MEDICAL SYSTEMS ADULT ANES BREATH 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 Merit Medical Systems, 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.

K261310FlexTract Deflectable-Rotational Dilator Sheath SetK262086PreludeSYNC™ Radial Compression DeviceK254073StatSeal DiscK251802STAR RF Ablation SystemK252892SCOUT MD Surgical Guidance SystemK250853Merit Syringe

View all 159 devices →

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.

↑