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)

BLUE RIDGE RABBIT BLOOD

K-Number: K820849 · 1982-04-16

ApplicantBlue Ridge Media Co.
Decision Date1982-04-16
Product CodeLHW
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

BLUE RIDGE RABBIT BLOOD is the device name listed in this FDA 510(k) record. The listed applicant is Blue Ridge Media Co.. It received FDA 510(k) clearance on 1982-04-16 under 510(k) number K820849. The device is classified under product code LHW. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BLUE RIDGE RABBIT BLOOD?

BLUE RIDGE RABBIT BLOOD is a medical device that received FDA 510(k) clearance on 1982-04-16. The listed applicant is Blue Ridge Media Co.. The 510(k) number is K820849.

When did BLUE RIDGE RABBIT BLOOD receive FDA 510(k) clearance?

BLUE RIDGE RABBIT BLOOD received FDA 510(k) clearance on 1982-04-16, under 510(k) number K820849.

Who is the listed applicant for BLUE RIDGE RABBIT BLOOD?

The FDA 510(k) record lists Blue Ridge Media Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BLUE RIDGE RABBIT BLOOD?

The FDA product code for BLUE RIDGE RABBIT BLOOD is LHW.

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 Blue Ridge Media 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.

K820848BLUE RIDGE SHEEP BLOODK820840CULTURE MEDIA, GENERAL NUTRIENT BROTHK820845DULTURE MEDIA, SELECTIVE & NON-DIFFERK820847ISOLATION OF PATHOGENIC NEISSERIAK820842CULTURE MEDIA, NON-SELECTIVE/DIFFERK820844CULTURE MEDIA, SELECTIVE & DIFFERENTIAL

View all 11 devices →

Related Devices (Code: LHW)

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.

K820848BLUE RIDGE SHEEP BLOODBlue Ridge Media Co.K813513AFRICAN GREEN MONKEY BLOOD IN ALSERVERSDutchland Laboratories, Inc.K813512RHESUS MONKEY BLOOD IN ALSEVER'SDutchland Laboratories, 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.

↑