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)

C.A.S.E. CONTAINER

K-Number: K844652 · 1984-12-12

ApplicantGeneral Medical Co.
Decision Date1984-12-12
Product CodeFSM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

C.A.S.E. CONTAINER is the device name listed in this FDA 510(k) record. The listed applicant is General Medical Co.. It received FDA 510(k) clearance on 1984-12-12 under 510(k) number K844652. The device is classified under product code FSM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the C.A.S.E. CONTAINER?

C.A.S.E. CONTAINER is a medical device that received FDA 510(k) clearance on 1984-12-12. The listed applicant is General Medical Co.. The 510(k) number is K844652.

When did C.A.S.E. CONTAINER receive FDA 510(k) clearance?

C.A.S.E. CONTAINER received FDA 510(k) clearance on 1984-12-12, under 510(k) number K844652.

Who is the listed applicant for C.A.S.E. CONTAINER?

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

What is the FDA product code for C.A.S.E. CONTAINER?

The FDA product code for C.A.S.E. CONTAINER is FSM.

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 General Medical 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.

K926269PROCEDURE KITK912975OPERAND LUBRICATING JELLYK912132OPERAND LUBRICATING JELLYK903669GENESIS INSUFFLATING CATHETERK900110OPERAND* LUBRICATING JELLYK853635SUBDERM TM

View all 15 devices →

Related Devices (Code: FSM)

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.

K971217INSTRUMENT TRAY LINERGeneral Hospital Supply Corp.K962328SINGLE USE INSTRUMENT TRAYMedcare Medical Group, Inc.K944025SURGICAL INSTRUMENT TRAYRiley Medical, Inc.K912106ARTHROSCOPY TRAYMedical Device Inspection Co., Inc.K912053OPEN HEART TRAYMedical Device Inspection Co., Inc.K912052HEART CATH TRAYMedical Device Inspection Co., 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.

↑