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)

GRAVITY KING (DEEMED SE 87/09/18)

K-Number: K851065 · 1985-06-13

ApplicantUnique Functional Products
Decision Date1985-06-13
Product CodeION
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

GRAVITY KING (DEEMED SE 87/09/18) is the device name listed in this FDA 510(k) record. The listed applicant is Unique Functional Products. It received FDA 510(k) clearance on 1985-06-13 under 510(k) number K851065. The device is classified under product code ION. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GRAVITY KING (DEEMED SE 87/09/18)?

GRAVITY KING (DEEMED SE 87/09/18) is a medical device that received FDA 510(k) clearance on 1985-06-13. The listed applicant is Unique Functional Products. The 510(k) number is K851065.

When did GRAVITY KING (DEEMED SE 87/09/18) receive FDA 510(k) clearance?

GRAVITY KING (DEEMED SE 87/09/18) received FDA 510(k) clearance on 1985-06-13, under 510(k) number K851065.

Who is the listed applicant for GRAVITY KING (DEEMED SE 87/09/18)?

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

What is the FDA product code for GRAVITY KING (DEEMED SE 87/09/18)?

The FDA product code for GRAVITY KING (DEEMED SE 87/09/18) is ION.

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

Related Devices (Code: ION)

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.

K120783ABLE-XIm-Able, Ltd.K885343STANDEXAlt, Inc.K840551MOBILIZERLossing Orthopedic, Inc.K833870KNEE WALKERMaddak, Inc.K833249FITNESSFitness Equipment Co., Inc.K832968PEDAL EXERCISERMaddak, 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.

↑