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)

WATCHCHILD OBSTERICAL PATIENT DATA MANAGEMENT SYSTEM

K-Number: K974248 · 1998-10-07

ApplicantAir-Shields, Inc.
Decision Date1998-10-07
Product CodeHGM
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

WATCHCHILD OBSTERICAL PATIENT DATA MANAGEMENT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Air-Shields, Inc.. It received FDA 510(k) clearance on 1998-10-07 under 510(k) number K974248. The device is classified under product code HGM. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WATCHCHILD OBSTERICAL PATIENT DATA MANAGEMENT SYSTEM?

WATCHCHILD OBSTERICAL PATIENT DATA MANAGEMENT SYSTEM is a medical device that received FDA 510(k) clearance on 1998-10-07. The listed applicant is Air-Shields, Inc.. The 510(k) number is K974248.

When did WATCHCHILD OBSTERICAL PATIENT DATA MANAGEMENT SYSTEM receive FDA 510(k) clearance?

WATCHCHILD OBSTERICAL PATIENT DATA MANAGEMENT SYSTEM received FDA 510(k) clearance on 1998-10-07, under 510(k) number K974248.

Who is the listed applicant for WATCHCHILD OBSTERICAL PATIENT DATA MANAGEMENT SYSTEM?

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

What is the FDA product code for WATCHCHILD OBSTERICAL PATIENT DATA MANAGEMENT SYSTEM?

The FDA product code for WATCHCHILD OBSTERICAL PATIENT DATA MANAGEMENT SYSTEM is HGM.

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 Air-Shields, 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.

K972309JM-102 JAUNDICE METERK971256DUO-LITE PHOTOTHERAPY SYSTEMK960980ISOLETTE INFANT INCUBATORK924709SATCARE OXYGEN CONTROLLER/MONITOR W/ PULSE OXIMETEK940951RW RESUCITAIRE INFANT RADIANT WARMERK940975C450/C400 INFANT INCUBATORS

View all 33 devices →

Related Devices (Code: HGM)

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.

K254036Novii+ Wireless Patch SystemDatex Ohmeda, Inc.K253021ANNE MaternalSibel Health, Inc.K250777Sonicaid Team3Huntleigh Healthcare , Ltd.K241882Fetal & Maternal Monitor (F15A, F15A Air)Edan Instruments, Inc.K241368Sonicaid Team3Huntleigh Healthcare , Ltd.K241009PeriCALM Patterns 3.0Perigen, 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.

↑