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FDA 510(k)

PERSONAL BODY MASSAGER, MODELS 1605 & 1606

K-Number: K912822 · 1992-02-11

ApplicantRaymond Industrial, Ltd.
Decision Date1992-02-11
Product CodeISA
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PERSONAL BODY MASSAGER, MODELS 1605 & 1606 is the device name listed in this FDA 510(k) record. The listed applicant is Raymond Industrial, Ltd.. It received FDA 510(k) clearance on 1992-02-11 under 510(k) number K912822. 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 PERSONAL BODY MASSAGER, MODELS 1605 & 1606?

PERSONAL BODY MASSAGER, MODELS 1605 & 1606 is a medical device that received FDA 510(k) clearance on 1992-02-11. The listed applicant is Raymond Industrial, Ltd.. The 510(k) number is K912822.

When did PERSONAL BODY MASSAGER, MODELS 1605 & 1606 receive FDA 510(k) clearance?

PERSONAL BODY MASSAGER, MODELS 1605 & 1606 received FDA 510(k) clearance on 1992-02-11, under 510(k) number K912822.

Who is the listed applicant for PERSONAL BODY MASSAGER, MODELS 1605 & 1606?

The FDA 510(k) record lists Raymond Industrial, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PERSONAL BODY MASSAGER, MODELS 1605 & 1606?

The FDA product code for PERSONAL BODY MASSAGER, MODELS 1605 & 1606 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 Raymond Industrial, Ltd. 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.

K022626MOISTURESTAY (REVLON)

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

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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