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)

PALMER OBSTETRIC BRACE

K-Number: K864194 · 1987-01-14

ApplicantAd-Tech Medical Instrument Corp
Decision Date1987-01-14
Product CodeKNC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

PALMER OBSTETRIC BRACE is the device name listed in this FDA 510(k) record. The listed applicant is Ad-Tech Medical Instrument Corp. It received FDA 510(k) clearance on 1987-01-14 under 510(k) number K864194. The device is classified under product code KNC. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PALMER OBSTETRIC BRACE?

PALMER OBSTETRIC BRACE is a medical device that received FDA 510(k) clearance on 1987-01-14. The listed applicant is Ad-Tech Medical Instrument Corp. The 510(k) number is K864194.

When did PALMER OBSTETRIC BRACE receive FDA 510(k) clearance?

PALMER OBSTETRIC BRACE received FDA 510(k) clearance on 1987-01-14, under 510(k) number K864194.

Who is the listed applicant for PALMER OBSTETRIC BRACE?

The FDA 510(k) record lists Ad-Tech Medical Instrument Corp as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PALMER OBSTETRIC BRACE?

The FDA product code for PALMER OBSTETRIC BRACE is KNC.

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 Ad-Tech Medical Instrument 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.

K112094BRAIN BIOPSY NEEDLEK053363DUAL-SIDED INTERHEMISPHERIC SUBDURAL ELECTRODES, GRID SUBDURAL ELECTRODES, INTRAOPERATIVE SUBDURAL ELECTRODESK053358DEPTH ELECTRODE, FORAMEN OVALE DEPTH ELECTRODES, WYLER SPHENOIDAL DEPTH ELECTRODESK041604MACRO-MICRO DEPTH ELECTRODEK990788AD-TECH'S FORAMEN OVALE ELECTRODEK992194CORTICAL MAPPING UNIT, MODEL CMU

View all 18 devices →

Related Devices (Code: KNC)

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.

K001261L720 EXAMINATION CHAIRLuneau Gynecologie SAK932035NON-LINTING DELIVERY BLANKETAmsco Sterile Recoveries, Inc.K924420MEDICAL DISPOSABLE BEDDINGHill-Rom, Inc.K914544BD6000 THE OPTIMA & BD5000 BIRTHING BEDLic Care, Inc.K915779AFFINITY BED MODEL 3600 SERIESHill-Rom, Inc.K903973GARDOSI BIRTHING CUSHIONGraphic Controls 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.

↑