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)

BNS 40

K-Number: K842224 · 1984-11-19

ApplicantMyo-Tronics Research, Inc.
Decision Date1984-11-19
Product CodeNUW
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

BNS 40 is the device name listed in this FDA 510(k) record. The listed applicant is Myo-Tronics Research, Inc.. It received FDA 510(k) clearance on 1984-11-19 under 510(k) number K842224. The device is classified under product code NUW. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BNS 40?

BNS 40 is a medical device that received FDA 510(k) clearance on 1984-11-19. The listed applicant is Myo-Tronics Research, Inc.. The 510(k) number is K842224.

When did BNS 40 receive FDA 510(k) clearance?

BNS 40 received FDA 510(k) clearance on 1984-11-19, under 510(k) number K842224.

Who is the listed applicant for BNS 40?

The FDA 510(k) record lists Myo-Tronics Research, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BNS 40?

The FDA product code for BNS 40 is NUW.

Other records listing Myo-Tronics Research, 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.

K842223J4 MYO-MONITORK833132MUCOSAL ADJUSTMENT PASTE LIQUID SPRAYK831364TESTCORP RAK830034MODEL EM-2 BIOELECTRIC PROCESSORK813533ELECTRIC MUSCLE STIMULATORK810528MODEL EM-IR

View all 8 devices →

Related Devices (Code: NUW)

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.

K243290BTL-785MJBTL Industries, Inc.K203525D functionIto Co., Ltd.K040400MYO-TRODE SG DISPOSABLE ELECTRODEMyotronics-Noromed, Inc.K031998MODEL J-5 MVO-MONITORMyotronics-Noromed, Inc.K901902ACUSOURCE 600 FOR USE WITH TMJ ELECTRODEMicrocurrent Research, Inc.K890143ACUTRON MULTIWAVE FOR USE IN TMJ SYNDROME PAIN CONMicrocurrent Research, 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.

↑