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)

MULTIPLE(HEMORX) IF APPROVED BY TRADEMARK OFFICE

K-Number: K852679 · 1985-08-09

ApplicantJ. & Jp., Inc.
Decision Date1985-08-09
Product CodeLKX
DecisionSubstantially Equivalent

Device Summary

MULTIPLE(HEMORX) IF APPROVED BY TRADEMARK OFFICE is the device name listed in this FDA 510(k) record. The listed applicant is J. & Jp., Inc.. It received FDA 510(k) clearance on 1985-08-09 under 510(k) number K852679. The device is classified under product code LKX. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTIPLE(HEMORX) IF APPROVED BY TRADEMARK OFFICE?

MULTIPLE(HEMORX) IF APPROVED BY TRADEMARK OFFICE is a medical device that received FDA 510(k) clearance on 1985-08-09. The listed applicant is J. & Jp., Inc.. The 510(k) number is K852679.

When did MULTIPLE(HEMORX) IF APPROVED BY TRADEMARK OFFICE receive FDA 510(k) clearance?

MULTIPLE(HEMORX) IF APPROVED BY TRADEMARK OFFICE received FDA 510(k) clearance on 1985-08-09, under 510(k) number K852679.

Who is the listed applicant for MULTIPLE(HEMORX) IF APPROVED BY TRADEMARK OFFICE?

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

What is the FDA product code for MULTIPLE(HEMORX) IF APPROVED BY TRADEMARK OFFICE?

The FDA product code for MULTIPLE(HEMORX) IF APPROVED BY TRADEMARK OFFICE is LKX.

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 J. & Jp., 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.

K862490ANU-RX

Related Devices (Code: LKX)

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.

K172358InstaliefPrivi Medical Pte, Ltd.K113660COLD PACK, PLASTIC APPLICATOR (MEDICAL GRADE)-NON-CHEMICALCryotherapy Products, Inc.K072414CRYOSTATLil Drug Store Products, Inc.K042564HEMOR-RITE CRYOTHERAPHYFama Holdings International CorpK012746ICE BATONBehive, Ltd.K981428ANU ICECryoptherapy Pain Relief Products, 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.

↑