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FDA 510(k)

UPACS VERSION 1.7

K-Number: K961160 · 1996-06-11

ApplicantBase Ten Systems, Inc.
Decision Date1996-06-11
Product CodeLMB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

UPACS VERSION 1.7 is the device name listed in this FDA 510(k) record. The listed applicant is Base Ten Systems, Inc.. It received FDA 510(k) clearance on 1996-06-11 under 510(k) number K961160. 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 UPACS VERSION 1.7?

UPACS VERSION 1.7 is a medical device that received FDA 510(k) clearance on 1996-06-11. The listed applicant is Base Ten Systems, Inc.. The 510(k) number is K961160.

When did UPACS VERSION 1.7 receive FDA 510(k) clearance?

UPACS VERSION 1.7 received FDA 510(k) clearance on 1996-06-11, under 510(k) number K961160.

Who is the listed applicant for UPACS VERSION 1.7?

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

What is the FDA product code for UPACS VERSION 1.7?

The FDA product code for UPACS VERSION 1.7 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 Base Ten Systems, 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.

K960941UPACSK953652PRENVAL I

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

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