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)

REGULATOR FLOWMETER

K-Number: K915505 · 1992-04-22

ApplicantLifeguard Medical Products, Inc.
Decision Date1992-04-22
Product CodeCAN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

REGULATOR FLOWMETER is the device name listed in this FDA 510(k) record. The listed applicant is Lifeguard Medical Products, Inc.. It received FDA 510(k) clearance on 1992-04-22 under 510(k) number K915505. The device is classified under product code CAN. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REGULATOR FLOWMETER?

REGULATOR FLOWMETER is a medical device that received FDA 510(k) clearance on 1992-04-22. The listed applicant is Lifeguard Medical Products, Inc.. The 510(k) number is K915505.

When did REGULATOR FLOWMETER receive FDA 510(k) clearance?

REGULATOR FLOWMETER received FDA 510(k) clearance on 1992-04-22, under 510(k) number K915505.

Who is the listed applicant for REGULATOR FLOWMETER?

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

What is the FDA product code for REGULATOR FLOWMETER?

The FDA product code for REGULATOR FLOWMETER is CAN.

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 Lifeguard Medical Products, 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.

K013421LIFEGUARD NASAL CPAP MASK AND ACCESSORIESK915296MONOPOLAR ELECTRODEK920471LEVY ARTICULATING RETRACTORK915297TROCAR & TROCAR SLEEEVE 11MM, 10MM, 8MM & 5MMK915298SUCTION/IRRIGATION CANNULA; CATLOG #532.00K880958LIFEGUARD BACTERIAL AND VIRAL FILTER

View all 12 devices →

Related Devices (Code: CAN)

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.

K162811MR Conditional CGA 870Essex Industries, Inc.K080243PORTABLE OXYGEN UNIT SCA900San Cheong Co. , Ltd.K060265REMCORE REMOTE CONTROLLED OXYGEN REGULATORRemcore, Inc.K061785CYL-FIL OXYGEN SYSTEMResponsive Respiratory, Inc.K950777OXYGEN REGULATORMada Medical Products, Inc.K942751VANGUARD SERIES GAS REGULATORSBuckman Co., 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.

↑