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FDA 510(k)

BC (BODY COMPOSITION SOFTWARE)

K-Number: K070999 · 2007-08-02

ApplicantRjl Systems, Inc.
Decision Date2007-08-02
Product CodeMNW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BC (BODY COMPOSITION SOFTWARE) is the device name listed in this FDA 510(k) record. The listed applicant is Rjl Systems, Inc.. It received FDA 510(k) clearance on 2007-08-02 under 510(k) number K070999. The device is classified under product code MNW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BC (BODY COMPOSITION SOFTWARE)?

BC (BODY COMPOSITION SOFTWARE) is a medical device that received FDA 510(k) clearance on 2007-08-02. The listed applicant is Rjl Systems, Inc.. The 510(k) number is K070999.

When did BC (BODY COMPOSITION SOFTWARE) receive FDA 510(k) clearance?

BC (BODY COMPOSITION SOFTWARE) received FDA 510(k) clearance on 2007-08-02, under 510(k) number K070999.

Who is the listed applicant for BC (BODY COMPOSITION SOFTWARE)?

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

What is the FDA product code for BC (BODY COMPOSITION SOFTWARE)?

The FDA product code for BC (BODY COMPOSITION SOFTWARE) is MNW.

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 Rjl 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.

K911194IMPEDANCE PHLEBOGRAPH/PHOTOPLETHYSMOGRAPH-DVT-2000K862383MODIFIED MODEL BIA-103 BODY COMPOSITION ANALYZERK830292BIOELECTRICAL IMPEDANCE ANALYZER #101

Related Devices (Code: MNW)

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.

K231116Multi-parameter detectorZhongshan Jinli Electronic Weighing Equipment Co., Ltd.K130856BIA / VITALITY ANALYZERIpgdx, LLCK130777INBODYBiospace Corporation LimitedK130952PRECISION ONE LIFECARE; DETECTO; DETECTOPrecision One Lifecare, Ltd.K131394TRANSTEK GLASS BODY FAT ANALYZERGuangdong Transtek Medical Electronics Co., Ltd.K130311TRANSTEK BODY FAT ANALYZERGuangdong Transtek Medical Electronics Co., Ltd.

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.

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