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FDA 510(k)

SPINAL PAD

K-Number: K993684 · 2000-07-19

ApplicantBioscan, Inc.
Decision Date2000-07-19
Product CodeILY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SPINAL PAD is the device name listed in this FDA 510(k) record. The listed applicant is Bioscan, Inc.. It received FDA 510(k) clearance on 2000-07-19 under 510(k) number K993684. The device is classified under product code ILY. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPINAL PAD?

SPINAL PAD is a medical device that received FDA 510(k) clearance on 2000-07-19. The listed applicant is Bioscan, Inc.. The 510(k) number is K993684.

When did SPINAL PAD receive FDA 510(k) clearance?

SPINAL PAD received FDA 510(k) clearance on 2000-07-19, under 510(k) number K993684.

Who is the listed applicant for SPINAL PAD?

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

What is the FDA product code for SPINAL PAD?

The FDA product code for SPINAL PAD is ILY.

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 Bioscan, 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.

K993686LIGHT PATCHK993685BIOPACK

Related Devices (Code: ILY)

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.

K253965CureLight Medical Diode Laser Systems (CureLight F2-A15; CureLight F2-B15; CureLight F2-A30; CureLight F2-B30; CureLight F3-AB30; CureLight F3-AB60.)Wuhan PHOMED Technology Company , Ltd.K242755Medical Diode Laser Systems (VELAS II-30B, VELAS II-30A, GBOX-15AB, GBOX-20B, CHEESE II-10B)Gigaalaser Company , Ltd.K231997SIRONA 100 Therapy Laser System (OEM's Model EVANLAS)Cure Point Therapeutics, Inc.K223642LED Lip Perfector, model: ZC-05Light Tree Ventures Europe B.V.K221189OLIZ LTB-1000ALtbio Co., Ltd.K213524CytonPro-5000Cytonsys, Inc.

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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