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 PETRI DISH

K-Number: K843483 · 1984-09-21

ApplicantZimmar Consulting , Ltd.
Decision Date1984-09-21
Product CodeLIB
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

PHARMA-PLAST PETRI DISH 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 1984-09-21 under 510(k) number K843483. The device is classified under product code LIB. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHARMA-PLAST PETRI DISH?

PHARMA-PLAST PETRI DISH is a medical device that received FDA 510(k) clearance on 1984-09-21. The listed applicant is Zimmar Consulting , Ltd.. The 510(k) number is K843483.

When did PHARMA-PLAST PETRI DISH receive FDA 510(k) clearance?

PHARMA-PLAST PETRI DISH received FDA 510(k) clearance on 1984-09-21, under 510(k) number K843483.

Who is the listed applicant for PHARMA-PLAST PETRI DISH?

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 PETRI DISH?

The FDA product code for PHARMA-PLAST PETRI DISH is LIB.

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-URIDOMEK843468PHARMA-PLAST SUCTION SET TYPE YANKAUERK843466PHARMA-PLAST OXYGEN CATHETERK843469PHARMA-PLAST SUCTION TIP, TYPE ORTHOPAE-

View all 17 devices →

Related Devices (Code: LIB)

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.

K023677OSMETECH MICROBIAL ANALYSER-BACTERIAL VAGINOSIS (OMA-BV)OsmetechK920416SUPPLEMENTARY REAGENTS FOR ENZYGNOST/TMBBehring Diagnostics, Inc.K912558GULL ELISAWAREGull Laboratories, Inc.K872273CORNING EASY WASH ELISA PLATESCorning Medical & ScientificK871559CELL LIFTERCorning Costar Corp.K864249NORMAL SALINE STERILEMds Laboratories, 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.

↑