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)

MDT/CASTLE 10/90 LOAD STATION

K-Number: K910649 · 1991-09-06

ApplicantMdt Biologic Co.
Decision Date1991-09-06
Product CodeFLF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MDT/CASTLE 10/90 LOAD STATION is the device name listed in this FDA 510(k) record. The listed applicant is Mdt Biologic Co.. It received FDA 510(k) clearance on 1991-09-06 under 510(k) number K910649. The device is classified under product code FLF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MDT/CASTLE 10/90 LOAD STATION?

MDT/CASTLE 10/90 LOAD STATION is a medical device that received FDA 510(k) clearance on 1991-09-06. The listed applicant is Mdt Biologic Co.. The 510(k) number is K910649.

When did MDT/CASTLE 10/90 LOAD STATION receive FDA 510(k) clearance?

MDT/CASTLE 10/90 LOAD STATION received FDA 510(k) clearance on 1991-09-06, under 510(k) number K910649.

Who is the listed applicant for MDT/CASTLE 10/90 LOAD STATION?

The FDA 510(k) record lists Mdt Biologic Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MDT/CASTLE 10/90 LOAD STATION?

The FDA product code for MDT/CASTLE 10/90 LOAD STATION is FLF.

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 Mdt Biologic Co. 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.

K954736ACCESS (POWERCLAVE)K954940MDT STERIGRIP DISPOSABLE, SOFT COVER, LIGHT HANDLEK943654HARVEY CHEMICLAVE EC5000, EC5500, EC6000 STERILIZERSK911087CASTLE WASHER/DISINFECTOR, MODEL 7550K910777MDT/CASTLE MODELS S-8 TABLE TOP STEAM STERILIZERK910778STEAM VACUUM PULSE STERILIZER SYSTEM (SVPSS)

View all 8 devices →

Related Devices (Code: FLF)

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.

K192978EOGas 4 Ethylene Oxide Gas SterilizerAndersen Sterilizers, Inc.K170432Anprolene AN75 Ethylene Oxide Gas SterilizerAndersen Sterilizers, Inc.K090636TSO3 OZONE STERILIZER, MODEL 125LTso3, Inc.K051595TSO3 OZONE STERILIZER, MODEL 125LTso3, Inc.K020875TSO3 OZONE STERILIZER, MODEL 125LTechnologies of Sterilization With Oxone, Tso3, Inc.K014013H & W HOSPITAL ETHYLENE OXIDE STERILIZER CONTROL SYSTEMH & W Technology, LLC

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.

↑