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)

COSMEDTECH CANNULA

K-Number: K870560 · 1987-03-04

ApplicantCosmedtech, Inc.
Decision Date1987-03-04
Product CodeHHI
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

COSMEDTECH CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Cosmedtech, Inc.. It received FDA 510(k) clearance on 1987-03-04 under 510(k) number K870560. The device is classified under product code HHI. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COSMEDTECH CANNULA?

COSMEDTECH CANNULA is a medical device that received FDA 510(k) clearance on 1987-03-04. The listed applicant is Cosmedtech, Inc.. The 510(k) number is K870560.

When did COSMEDTECH CANNULA receive FDA 510(k) clearance?

COSMEDTECH CANNULA received FDA 510(k) clearance on 1987-03-04, under 510(k) number K870560.

Who is the listed applicant for COSMEDTECH CANNULA?

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

What is the FDA product code for COSMEDTECH CANNULA?

The FDA product code for COSMEDTECH CANNULA is HHI.

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 Cosmedtech, 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.

K873552CANNULA AND GENERAL PURPOSE ASPIRATORK870574COSMEDTECH GENERAL ASPIRATOR

Related Devices (Code: HHI)

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.

K171440Berkeley VC-10 Vacuum Curettage SystemGyrus AcmiK030935BERKELEY V-10 VACUUM CURETTAGE SYSTEMAcmi CorporationK983181CYTOPREPCytoprep Inc. Est.K931205MEDI VAC SPECIMEN COLLECTOR AND TRANSPORTERBaxter Healthcare CorpK904160CYTOSMEAR BRUSHBrooke Intl.K900641CANNULA, SUCTION UTERINEWilliams Specialty Products, 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.

↑