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)

HEAD FACILITATION VIBRATOR BK-5210

K-Number: K771279 · 1977-08-26

ApplicantFred Sammons, Inc.
Decision Date1977-08-26
Product CodeIRO
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

HEAD FACILITATION VIBRATOR BK-5210 is the device name listed in this FDA 510(k) record. The listed applicant is Fred Sammons, Inc.. It received FDA 510(k) clearance on 1977-08-26 under 510(k) number K771279. 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 HEAD FACILITATION VIBRATOR BK-5210?

HEAD FACILITATION VIBRATOR BK-5210 is a medical device that received FDA 510(k) clearance on 1977-08-26. The listed applicant is Fred Sammons, Inc.. The 510(k) number is K771279.

When did HEAD FACILITATION VIBRATOR BK-5210 receive FDA 510(k) clearance?

HEAD FACILITATION VIBRATOR BK-5210 received FDA 510(k) clearance on 1977-08-26, under 510(k) number K771279.

Who is the listed applicant for HEAD FACILITATION VIBRATOR BK-5210?

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

What is the FDA product code for HEAD FACILITATION VIBRATOR BK-5210?

The FDA product code for HEAD FACILITATION VIBRATOR BK-5210 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 Fred Sammons, 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.

K880644ULTRA-PAN FOR ORTHOTIC PLASTICS (7262)K880647ADULT PERCEPTUAL MOTOR PUZZLES (5331-01)K831549ARM SLINGSK831548SPLINTSK831550FINGER BONIOMETER BK7506K831544DELUXE TRACTION EXERCISE GLOVE BK5035

View all 278 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.K950441CONAIR FAMILY FITNESS BODY ENERGYConair Corp.

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.

↑