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)

SRT-SYSTEM

K-Number: K852554 · 1985-07-18

ApplicantMicrowave Development, Inc.
Decision Date1985-07-18
Product CodeJPH
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

SRT-SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Microwave Development, Inc.. It received FDA 510(k) clearance on 1985-07-18 under 510(k) number K852554. The device is classified under product code JPH. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SRT-SYSTEM?

SRT-SYSTEM is a medical device that received FDA 510(k) clearance on 1985-07-18. The listed applicant is Microwave Development, Inc.. The 510(k) number is K852554.

When did SRT-SYSTEM receive FDA 510(k) clearance?

SRT-SYSTEM received FDA 510(k) clearance on 1985-07-18, under 510(k) number K852554.

Who is the listed applicant for SRT-SYSTEM?

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

What is the FDA product code for SRT-SYSTEM?

The FDA product code for SRT-SYSTEM is JPH.

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

Related Devices (Code: JPH)

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.

K871076WINPETTEUlster Scientific, Inc.K860899DISPETTE IIUlster Scientific, Inc.K840500SEDIPLASTPrecision Technology, Inc.K831195WESTERGREN DISPETTE FOR ESRUlster Scientific, Inc.K823761ERYTHROCYTE & STAND SEDIMENT. RATE TUBECordis Corp.K823368DADE ESR KITAmerican Dade

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.

↑