FDA 510(k)

CERVICAL ORTHOPEDIC PILLOW

K-Number: K791757 · 1979-10-01

Decision Date1979-10-01

Product Code

DecisionSubstantially Equivalent

Device Summary

CERVICAL ORTHOPEDIC PILLOW is the device name listed in this FDA 510(k) record. The listed applicant is Adeline V. Santoro. It received FDA 510(k) clearance on 1979-10-01 under 510(k) number K791757. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CERVICAL ORTHOPEDIC PILLOW?

CERVICAL ORTHOPEDIC PILLOW is a medical device that received FDA 510(k) clearance on 1979-10-01. The listed applicant is Adeline V. Santoro. The 510(k) number is K791757.

When did CERVICAL ORTHOPEDIC PILLOW receive FDA 510(k) clearance?

CERVICAL ORTHOPEDIC PILLOW received FDA 510(k) clearance on 1979-10-01, under 510(k) number K791757.

Who is the listed applicant for CERVICAL ORTHOPEDIC PILLOW?

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

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_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.