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FDA 510(k)

CORDLESS ELECTRIC MASSAGER EV315

K-Number: K912634 · 1991-09-12

ApplicantMatsushita Electric Co.
Decision Date1991-09-12
Product CodeISA
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CORDLESS ELECTRIC MASSAGER EV315 is the device name listed in this FDA 510(k) record. The listed applicant is Matsushita Electric Co.. It received FDA 510(k) clearance on 1991-09-12 under 510(k) number K912634. The device is classified under product code ISA. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CORDLESS ELECTRIC MASSAGER EV315?

CORDLESS ELECTRIC MASSAGER EV315 is a medical device that received FDA 510(k) clearance on 1991-09-12. The listed applicant is Matsushita Electric Co.. The 510(k) number is K912634.

When did CORDLESS ELECTRIC MASSAGER EV315 receive FDA 510(k) clearance?

CORDLESS ELECTRIC MASSAGER EV315 received FDA 510(k) clearance on 1991-09-12, under 510(k) number K912634.

Who is the listed applicant for CORDLESS ELECTRIC MASSAGER EV315?

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

What is the FDA product code for CORDLESS ELECTRIC MASSAGER EV315?

The FDA product code for CORDLESS ELECTRIC MASSAGER EV315 is ISA.

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.

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Other records listing Matsushita Electric 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.

K914198POWER FLOSS AND BRUSH EW 129 & EW 120

Related Devices (Code: ISA)

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.

K243488VMAT PROTermosaludK240358ShockPhysio Mobile (model SW3200 Basic)Shenzhen Dongdixin Technology Co., Ltd.K221865BTL-094BTL Industries, Inc.K210166Omnispec ED1000Medispec, Ltd.K213120OW100S (model OW100S-US)Tissue Regeneration Technologies, LLC Dba AS Softwave TrtK220538DolorClast RadialE.M.S Electro Medical Systems S.A

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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