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)

CONAIR FAMILY FITNESS BODY ENERGY

K-Number: K950441 · 1995-07-18

ApplicantConair Corp.
Decision Date1995-07-18
Product CodeIRO
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CONAIR FAMILY FITNESS BODY ENERGY is the device name listed in this FDA 510(k) record. The listed applicant is Conair Corp.. It received FDA 510(k) clearance on 1995-07-18 under 510(k) number K950441. The device is classified under product code IRO. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONAIR FAMILY FITNESS BODY ENERGY?

CONAIR FAMILY FITNESS BODY ENERGY is a medical device that received FDA 510(k) clearance on 1995-07-18. The listed applicant is Conair Corp.. The 510(k) number is K950441.

When did CONAIR FAMILY FITNESS BODY ENERGY receive FDA 510(k) clearance?

CONAIR FAMILY FITNESS BODY ENERGY received FDA 510(k) clearance on 1995-07-18, under 510(k) number K950441.

Who is the listed applicant for CONAIR FAMILY FITNESS BODY ENERGY?

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

What is the FDA product code for CONAIR FAMILY FITNESS BODY ENERGY?

The FDA product code for CONAIR FAMILY FITNESS BODY ENERGY is IRO.

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 Conair Corp. 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.

K950410CONAIR BODY AND SOLEK944637FAMILY FITNESS SHIATSU MASSAGERK943730SQUEEZE PLAYK924970FEMININE HEAT WRAPK943092FAMILY FITNESS SHIATSU MASSAGERK942950BODY FLEX

View all 29 devices →

Related Devices (Code: IRO)

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.

K955160COMFORT, MUSCLE, CORDLESS MASSAGER, BATTERY POWERED OPERATED MASSAGEREverapex Design & Marketing Corp.K955250QI GONG MASSAGEREast Health Development Group, Inc.K954203MASSAGER THERAPUTIC, ELECTRICCisco Sales Corp.K952916SHIATSU MASTER MASSAGER CUSHIONKinsei Shiatsu, Inc.K951414CHAMPION PHYSIOACOUSTICC RECLINER-TRANSPORTER CHAIRChampion Mfg. Corp.K946382SKALPI 3200Wiscco Development, 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.

↑