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)

FERNO WASHINGTON INCUBATOR TRANSPORTER, MOD. 35-IT

K-Number: K932417 · 1993-09-09

ApplicantFerno-Washington, Inc.
Decision Date1993-09-09
Product CodeFPL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FERNO WASHINGTON INCUBATOR TRANSPORTER, MOD. 35-IT is the device name listed in this FDA 510(k) record. The listed applicant is Ferno-Washington, Inc.. It received FDA 510(k) clearance on 1993-09-09 under 510(k) number K932417. The device is classified under product code FPL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FERNO WASHINGTON INCUBATOR TRANSPORTER, MOD. 35-IT?

FERNO WASHINGTON INCUBATOR TRANSPORTER, MOD. 35-IT is a medical device that received FDA 510(k) clearance on 1993-09-09. The listed applicant is Ferno-Washington, Inc.. The 510(k) number is K932417.

When did FERNO WASHINGTON INCUBATOR TRANSPORTER, MOD. 35-IT receive FDA 510(k) clearance?

FERNO WASHINGTON INCUBATOR TRANSPORTER, MOD. 35-IT received FDA 510(k) clearance on 1993-09-09, under 510(k) number K932417.

Who is the listed applicant for FERNO WASHINGTON INCUBATOR TRANSPORTER, MOD. 35-IT?

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

What is the FDA product code for FERNO WASHINGTON INCUBATOR TRANSPORTER, MOD. 35-IT?

The FDA product code for FERNO WASHINGTON INCUBATOR TRANSPORTER, MOD. 35-IT is FPL.

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 Ferno-Washington, 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.

K980033FERNO HEALTHCARE RECLINE-A-BATH 2K864765MODEL 668, TRACTION SPLINT, ADULTK864269MODEL 35-B ALL LEVEL COTK862441EZ LOAD MODEL 30, ALL LEVEL COT

Related Devices (Code: FPL)

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.

K220742NxtGen Infant Transport IncubatorInternational BiomedicalK161918SREE MRI Transport IncubatorAdvanced Imaging Research Dba Sree Medical SystemsK123937ATOM TRANSCAPSULE V-707Atom Medical CorporationK103523185A+ TRANSPORT INCUBATOR WITH MASIMO PULSEOX, 185A+ TRANSPORT INCUBATOR WITH NELLCOR PULSEOXInternational Biomedical, Ltd.K103525A750I TRANSPORT INCUBATOR WITH MASIMO PLUSEOX, A750I TRANSPORT INCUBATOR WITH NELLOR PULSEOXInternational Biomedical, Ltd.K103524VOYAGER TRANSPORT INCUBATOR WITH MASIMO PULSEOX, VOYAGER TRANSPORT INCUBATOR WITH NELLCOR PULSEOXInternational Biomedical, Ltd.

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.

↑