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)

FIBERGLASS CYLINDER BASES, #'S 65040-

K-Number: K800665 · 1980-04-02

ApplicantB & F Medical Products, Inc.
Decision Date1980-04-02
Product Code
DecisionSubstantially Equivalent

Device Summary

FIBERGLASS CYLINDER BASES, #'S 65040- is the device name listed in this FDA 510(k) record. The listed applicant is B & F Medical Products, Inc.. It received FDA 510(k) clearance on 1980-04-02 under 510(k) number K800665. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FIBERGLASS CYLINDER BASES, #'S 65040-?

FIBERGLASS CYLINDER BASES, #'S 65040- is a medical device that received FDA 510(k) clearance on 1980-04-02. The listed applicant is B & F Medical Products, Inc.. The 510(k) number is K800665.

When did FIBERGLASS CYLINDER BASES, #'S 65040- receive FDA 510(k) clearance?

FIBERGLASS CYLINDER BASES, #'S 65040- received FDA 510(k) clearance on 1980-04-02, under 510(k) number K800665.

Who is the listed applicant for FIBERGLASS CYLINDER BASES, #'S 65040-?

The FDA 510(k) record lists B & F Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

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 B & F Medical Products, 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.

K942645B&F MEDICAL OXYGEN REG MECICAL OXY COMPRESS GAS REGK920573CANNULA NASAL OXYGENK913501TRACHEOSTOMY MASKK861325MAXI-USE O2 DEVICEK861054DISPOSABLE RESCUE BREATHING DEVICEK853004PORTABLE OXYGEN UNIT

View all 18 devices →

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.

↑