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)

BRONCHOFIBERSCOPE, FB-19A

K-Number: K770879 · 1977-05-25

ApplicantPilling Co.
Decision Date1977-05-25
Product Code
DecisionSubstantially Equivalent

Device Summary

BRONCHOFIBERSCOPE, FB-19A is the device name listed in this FDA 510(k) record. The listed applicant is Pilling Co.. It received FDA 510(k) clearance on 1977-05-25 under 510(k) number K770879. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BRONCHOFIBERSCOPE, FB-19A?

BRONCHOFIBERSCOPE, FB-19A is a medical device that received FDA 510(k) clearance on 1977-05-25. The listed applicant is Pilling Co.. The 510(k) number is K770879.

When did BRONCHOFIBERSCOPE, FB-19A receive FDA 510(k) clearance?

BRONCHOFIBERSCOPE, FB-19A received FDA 510(k) clearance on 1977-05-25, under 510(k) number K770879.

Who is the listed applicant for BRONCHOFIBERSCOPE, FB-19A?

The FDA 510(k) record lists Pilling Co. 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 Pilling Co. 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.

K934427PILLING LAPAROSCOPIC INSTRUMENTATIONK925370TRIANGULAR JAW MICROLARYNGEAL FORCEPSK925198KAISER NO CANNULA THORACOSCOPY/LAPAROSCOPY INSTRK922971NO-SCALPEL VASCETOMY INSTRUMENTSK914015CLEMENT-PILLING CHOLANGIOGRAPHY CATH GUIDE/CLAMPK911099MEHIGAN-PILLING ANGIOSCOPIC VASCULAR INSTRUM. LINE

View all 39 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.

↑