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)

DISKCAM DC 6001

K-Number: K884148 · 1988-11-23

ApplicantCamtronics, Ltd.
Decision Date1988-11-23
Product CodeLMB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DISKCAM DC 6001 is the device name listed in this FDA 510(k) record. The listed applicant is Camtronics, Ltd.. It received FDA 510(k) clearance on 1988-11-23 under 510(k) number K884148. The device is classified under product code LMB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISKCAM DC 6001?

DISKCAM DC 6001 is a medical device that received FDA 510(k) clearance on 1988-11-23. The listed applicant is Camtronics, Ltd.. The 510(k) number is K884148.

When did DISKCAM DC 6001 receive FDA 510(k) clearance?

DISKCAM DC 6001 received FDA 510(k) clearance on 1988-11-23, under 510(k) number K884148.

Who is the listed applicant for DISKCAM DC 6001?

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

What is the FDA product code for DISKCAM DC 6001?

The FDA product code for DISKCAM DC 6001 is LMB.

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 Camtronics, 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.

K021236SURGERY AND ACCESSORIESK013032PHYSIOLOG, SERIES 95000K992666VIDEO PLUS SYSTEM, SERIES 95000K992259ECHOCARDIOGRAPHY SYSTEM SERIES 95000K990066CCD CAMERA, MODEL 9000K955519ANALYTICAL REVIEW STATION

View all 16 devices →

Related Devices (Code: LMB)

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.

K992131SAMSUNG RAYPAX LONG TERM ARCHIVESamsung Sds Co., Ltd.K984405ECHOLIVE FAMILY, MODELS: ZL-1010,ZL-2000,ZL-2100,ZL-3000,ZL-4000Intracom Corp.K983447WISE (II) IMAGE MANAGEMENT SYSTEMSectra-Imtec ABK980243PARAMETER DEVELOPMENTS DICOM ARCHIVAL SERVER, (DAS)/DICOM INTRANET SERVICE (DIS)Parameter Developments, Inc.K973463OLICON IMAGING SYSTEMS, INC. ARCHIVE SYSTEMS, NT ARCHIVE, 02ARCHIVE, ARCHIVEO Tech, Inc.K973413ID. STORE (RELEASE 2.0)I.S.G. Technologies, 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.

↑