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)

ScalpelCric

K-Number: K200190 · 2020-10-30

ApplicantVBM Medizintechnik GmbH
Decision Date2020-10-30
Product CodeBWC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ScalpelCric is the device name listed in this FDA 510(k) record. The listed applicant is VBM Medizintechnik GmbH. It received FDA 510(k) clearance on 2020-10-30 under 510(k) number K200190. The device is classified under product code BWC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ScalpelCric?

ScalpelCric is a medical device that received FDA 510(k) clearance on 2020-10-30. The listed applicant is VBM Medizintechnik GmbH. The 510(k) number is K200190.

When did ScalpelCric receive FDA 510(k) clearance?

ScalpelCric received FDA 510(k) clearance on 2020-10-30, under 510(k) number K200190.

Who is the listed applicant for ScalpelCric?

The FDA 510(k) record lists VBM Medizintechnik GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ScalpelCric?

The FDA product code for ScalpelCric is BWC.

Related Devices (Code: BWC)

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.

K160200Melker Cuffed Emergency Cricothyrotomy Catheter Sets, Melker Universal Cricothyrotomy Catheter SetCook IncorporatedK153761Emergency Transtracheal Airway CatheterCook Incorporated

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.

↑