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)

ADMINISTRATION SET

K-Number: K851988 · 1985-08-16

ApplicantTransamerica Delaval, Inc.
Decision Date1985-08-16
Product CodeDRS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ADMINISTRATION SET is the device name listed in this FDA 510(k) record. The listed applicant is Transamerica Delaval, Inc.. It received FDA 510(k) clearance on 1985-08-16 under 510(k) number K851988. The device is classified under product code DRS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADMINISTRATION SET?

ADMINISTRATION SET is a medical device that received FDA 510(k) clearance on 1985-08-16. The listed applicant is Transamerica Delaval, Inc.. The 510(k) number is K851988.

When did ADMINISTRATION SET receive FDA 510(k) clearance?

ADMINISTRATION SET received FDA 510(k) clearance on 1985-08-16, under 510(k) number K851988.

Who is the listed applicant for ADMINISTRATION SET?

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

What is the FDA product code for ADMINISTRATION SET?

The FDA product code for ADMINISTRATION SET is DRS.

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 Transamerica Delaval, 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.

K853996DISPOSABLE PRESSURE TRANSDUCER SYSTEM STERILEK851989DOME, DISPOSABLE, STERILEK851987FLUSH DEVICE, AUTOMATICK851986STOPCOCKSK833171MONITORING KITK833170FLUSH DEVICE

View all 7 devices →

Related Devices (Code: DRS)

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.

K254074TruPressProcerus EnterprisesK242909FloTrac sensors; FloTrac Jr sensors; Acumen IQ sensors; VolumeView sensorsEdwards Lifesciences, LLCK221782Meritrans ECO Reusable Pressure Transducer, Meritrans ECO DomesMerit Medical Pte. , Ltd.K172458HemoDraw Plus Closed Blood Sampling System with LogiCal Transducer Kit, HemoDraw Plus Closed Blood Sampling System with Transtar Transducer KitSmiths Medical Asd, Inc.K163172HemoDraw Plus Closed Blood Sampling System with LogiCal Transducer Kit, HemoDraw Plus Closed Blood Sampling System with Transtar Transducer KitSmiths Medical Asd, Inc.K161408Compass Cast and MAPCenturion Medical Products Corporation

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.

↑