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)

PMP, LTD. ADULT TEMP. MONITORING ANESTHESIA CIR.

K-Number: K932489 · 1993-07-22

ApplicantPrecision Med Products, Ltd.
Decision Date1993-07-22
Product CodeCAI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PMP, LTD. ADULT TEMP. MONITORING ANESTHESIA CIR. is the device name listed in this FDA 510(k) record. The listed applicant is Precision Med Products, Ltd.. It received FDA 510(k) clearance on 1993-07-22 under 510(k) number K932489. 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 PMP, LTD. ADULT TEMP. MONITORING ANESTHESIA CIR.?

PMP, LTD. ADULT TEMP. MONITORING ANESTHESIA CIR. is a medical device that received FDA 510(k) clearance on 1993-07-22. The listed applicant is Precision Med Products, Ltd.. The 510(k) number is K932489.

When did PMP, LTD. ADULT TEMP. MONITORING ANESTHESIA CIR. receive FDA 510(k) clearance?

PMP, LTD. ADULT TEMP. MONITORING ANESTHESIA CIR. received FDA 510(k) clearance on 1993-07-22, under 510(k) number K932489.

Who is the listed applicant for PMP, LTD. ADULT TEMP. MONITORING ANESTHESIA CIR.?

The FDA 510(k) record lists Precision Med Products, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PMP, LTD. ADULT TEMP. MONITORING ANESTHESIA CIR.?

The FDA product code for PMP, LTD. ADULT TEMP. MONITORING ANESTHESIA CIR. 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 Precision Med Products, Ltd. 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.

K932710GAS SAMPLING LINES AND CONNECTORSK932709PRECISION MED PRODUCTS LTD HYPERINFLATION SYSTEMK932707ADULT ANESTHESIA BREATHING CIRCUITK932708PRECISION MED PRODUCTS LTD MAPLESON D CIRCUITSK932711PRECISION MED PRODUCTS LTD GUEDEL AIRWAYSK932706PRECISION MED PRODUCTS LTD. VENTILATOR HOSE

View all 16 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.

↑