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FDA 510(k)

PEDICRAGT BASSINET

K-Number: K925949 · 1993-04-20

ApplicantPedicraft, Inc.
Decision Date1993-04-20
Product CodeFMS
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PEDICRAGT BASSINET is the device name listed in this FDA 510(k) record. The listed applicant is Pedicraft, Inc.. It received FDA 510(k) clearance on 1993-04-20 under 510(k) number K925949. The device is classified under product code FMS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PEDICRAGT BASSINET?

PEDICRAGT BASSINET is a medical device that received FDA 510(k) clearance on 1993-04-20. The listed applicant is Pedicraft, Inc.. The 510(k) number is K925949.

When did PEDICRAGT BASSINET receive FDA 510(k) clearance?

PEDICRAGT BASSINET received FDA 510(k) clearance on 1993-04-20, under 510(k) number K925949.

Who is the listed applicant for PEDICRAGT BASSINET?

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

What is the FDA product code for PEDICRAGT BASSINET?

The FDA product code for PEDICRAGT BASSINET is FMS.

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 Pedicraft, 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.

K925817HEAD & FOOT END DROP PEDI-CRIBK905630INFANT REFLUX SLINGK905629PEDICRAFT INFANT REFLUX WEDGEK821773PEDICRAFT BED, MODEL B2944

Related Devices (Code: FMS)

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.

K970334NATURE'S CRADLEInfant Advantage, Inc.K963210VAIL 100 PEDIATRIC CRIBVail Products, Inc.K960747NATURE'S CRADLE MODEL C1500Infant Advantage, Inc.K960012STRYKER ADEL BASSINETStryker Corp.K951024NATURE'S CRADLEInfant Advantage, Inc.K950059MC INFANT CARE UNIE #PP30Janco Consulting Services

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.

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