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FDA 510(k)

SPINE LINE

K-Number: K922366 · 1992-07-13

ApplicantDambrecine, Inc.
Decision Date1992-07-13
Product CodeLYG
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SPINE LINE is the device name listed in this FDA 510(k) record. The listed applicant is Dambrecine, Inc.. It received FDA 510(k) clearance on 1992-07-13 under 510(k) number K922366. The device is classified under product code LYG. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPINE LINE?

SPINE LINE is a medical device that received FDA 510(k) clearance on 1992-07-13. The listed applicant is Dambrecine, Inc.. The 510(k) number is K922366.

When did SPINE LINE receive FDA 510(k) clearance?

SPINE LINE received FDA 510(k) clearance on 1992-07-13, under 510(k) number K922366.

Who is the listed applicant for SPINE LINE?

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

What is the FDA product code for SPINE LINE?

The FDA product code for SPINE LINE is LYG.

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Related Devices (Code: LYG)

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.

K963704MUSCLE WAND, A DEVICE FOR DEEP PRESSURE MUSCLE MASSAGEShippert Medical Technologies Corp.K936312MANUAL MASSAGE ROLLERMckenna & CuneoK952043BACK MASSAGEREight Corners, Inc.K930613HOOKING SYSTEMAlain MachtelinckxK936148STRESS HANDLERArocep Enterprises , Ltd.K924315THE MASSAGERFour Directions

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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