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)

AM FAB SIDE RAILS MODEL 5000

K-Number: K852890 · 1985-07-24

ApplicantAm Fab, Inc.
Decision Date1985-07-24
Product CodeFNJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

AM FAB SIDE RAILS MODEL 5000 is the device name listed in this FDA 510(k) record. The listed applicant is Am Fab, Inc.. It received FDA 510(k) clearance on 1985-07-24 under 510(k) number K852890. The device is classified under product code FNJ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AM FAB SIDE RAILS MODEL 5000?

AM FAB SIDE RAILS MODEL 5000 is a medical device that received FDA 510(k) clearance on 1985-07-24. The listed applicant is Am Fab, Inc.. The 510(k) number is K852890.

When did AM FAB SIDE RAILS MODEL 5000 receive FDA 510(k) clearance?

AM FAB SIDE RAILS MODEL 5000 received FDA 510(k) clearance on 1985-07-24, under 510(k) number K852890.

Who is the listed applicant for AM FAB SIDE RAILS MODEL 5000?

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

What is the FDA product code for AM FAB SIDE RAILS MODEL 5000?

The FDA product code for AM FAB SIDE RAILS MODEL 5000 is FNJ.

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: FNJ)

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.

K934298KING KRIBNoritage, Inc.K892877CRADLE, HOSPITAL BED CLOTHINGWarsaw Orthopedic, Inc.K885241BED, ADJUSTABLE, HOSPITAL, FOLDING, FIELD, W/O MATKing Mfg. Co.K884542SIC 3999 FOLDING ADJUSTABLE HOSPITAL BEDCommercial Products & Engineering Co.K881725ENVIROTENT (BED)Envirotents, Inc.K881961MSI STANDARD BED MODELS: L1097-64 AND L1085-64Med Service, 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.

↑