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)

PILLOWPOSITIVE CERVICAL PILLOW

K-Number: K990871 · 1999-06-10

ApplicantLifesleep Systems, Inc.
Decision Date1999-06-10
Product CodeMYB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PILLOWPOSITIVE CERVICAL PILLOW is the device name listed in this FDA 510(k) record. The listed applicant is Lifesleep Systems, Inc.. It received FDA 510(k) clearance on 1999-06-10 under 510(k) number K990871. The device is classified under product code MYB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PILLOWPOSITIVE CERVICAL PILLOW?

PILLOWPOSITIVE CERVICAL PILLOW is a medical device that received FDA 510(k) clearance on 1999-06-10. The listed applicant is Lifesleep Systems, Inc.. The 510(k) number is K990871.

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

PILLOWPOSITIVE CERVICAL PILLOW received FDA 510(k) clearance on 1999-06-10, under 510(k) number K990871.

Who is the listed applicant for PILLOWPOSITIVE CERVICAL PILLOW?

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

What is the FDA product code for PILLOWPOSITIVE CERVICAL PILLOW?

The FDA product code for PILLOWPOSITIVE CERVICAL PILLOW is MYB.

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: MYB)

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.

K180608Lunoa SystemNightbalance BVK100160ZZOMA POSITIONAL SLEEPER MODEL 001Sleep Specialists, LLCK040161SONA PILLOWSleep Devices, Inc.K023010SNIFF POSITION PILLOWS/POPITZ PILLOWSAeolus International Corporation

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.

↑