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FDA 510(k)

MUCOSAL ADJUSTMENT PASTE LIQUID SPRAY

K-Number: K833132 · 1984-02-10

ApplicantMyo-Tronics Research, Inc.
Decision Date1984-02-10
Product CodeEFH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MUCOSAL ADJUSTMENT PASTE LIQUID SPRAY 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 1984-02-10 under 510(k) number K833132. The device is classified under product code EFH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MUCOSAL ADJUSTMENT PASTE LIQUID SPRAY?

MUCOSAL ADJUSTMENT PASTE LIQUID SPRAY is a medical device that received FDA 510(k) clearance on 1984-02-10. The listed applicant is Myo-Tronics Research, Inc.. The 510(k) number is K833132.

When did MUCOSAL ADJUSTMENT PASTE LIQUID SPRAY receive FDA 510(k) clearance?

MUCOSAL ADJUSTMENT PASTE LIQUID SPRAY received FDA 510(k) clearance on 1984-02-10, under 510(k) number K833132.

Who is the listed applicant for MUCOSAL ADJUSTMENT PASTE LIQUID SPRAY?

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 MUCOSAL ADJUSTMENT PASTE LIQUID SPRAY?

The FDA product code for MUCOSAL ADJUSTMENT PASTE LIQUID SPRAY is EFH.

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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.

K842224BNS 40K842223J4 MYO-MONITORK831364TESTCORP RAK830034MODEL EM-2 BIOELECTRIC PROCESSORK813533ELECTRIC MUSCLE STIMULATORK810528MODEL EM-IR

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Related Devices (Code: EFH)

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.

K965026PFINGST PRESSURE PASTEPfingst & Co., Inc.K912632OCCLUDEPascal Co., Inc.K911259HYDENTPascal Co., Inc.K864572FIXTECTORProdent Intl., Inc.K870032REVISED T-SCAN SYSTEMSentek, Inc.K832647ARTICULATING PAPERArdent Intl., 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.

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