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)

PHARMA-PLAST SUCTION SET TYPE YANKAUER

K-Number: K843468 · 1984-11-23

ApplicantZimmar Consulting , Ltd.
Decision Date1984-11-23
Product CodeGEA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PHARMA-PLAST SUCTION SET TYPE YANKAUER is the device name listed in this FDA 510(k) record. The listed applicant is Zimmar Consulting , Ltd.. It received FDA 510(k) clearance on 1984-11-23 under 510(k) number K843468. The device is classified under product code GEA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHARMA-PLAST SUCTION SET TYPE YANKAUER?

PHARMA-PLAST SUCTION SET TYPE YANKAUER is a medical device that received FDA 510(k) clearance on 1984-11-23. The listed applicant is Zimmar Consulting , Ltd.. The 510(k) number is K843468.

When did PHARMA-PLAST SUCTION SET TYPE YANKAUER receive FDA 510(k) clearance?

PHARMA-PLAST SUCTION SET TYPE YANKAUER received FDA 510(k) clearance on 1984-11-23, under 510(k) number K843468.

Who is the listed applicant for PHARMA-PLAST SUCTION SET TYPE YANKAUER?

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

What is the FDA product code for PHARMA-PLAST SUCTION SET TYPE YANKAUER?

The FDA product code for PHARMA-PLAST SUCTION SET TYPE YANKAUER is GEA.

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 Zimmar Consulting , Ltd. 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.

K860322CLINISET INFUSION SETK843477PHARMA-PLAST RECTAL TIPK843478PHARMA-PLAST URIDROP-URIDOMEK843467PHARMA-PLAST NASAL OXYGEN CANNULAK843466PHARMA-PLAST OXYGEN CATHETERK843469PHARMA-PLAST SUCTION TIP, TYPE ORTHOPAE-

View all 17 devices →

Related Devices (Code: GEA)

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.

K003965MRI SAFE INSTRUMENTSAesculap, Inc.K982472GENICON TROCARGenicon, LCK954599CONMED TROGARD ELECTRONIC TROCAR SYSTEMConmedcorpK922460ORIGIN SECONDARY CANNULA AND TROCAROrigin Medsystems, Inc.K920110ENDOPATH DISPOSABLE THORACIC TROCAR SLEEVEETHICON, Inc.K911262DISPOSABLE SPECIMEN BAG W/CANNULA AND INTRODUCERETHICON, 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.

↑