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FDA 510(k)

SOLSTICE XRAY RING MARKER PAD

K-Number: K925892 · 1993-05-18

ApplicantSolstice Corp.
Decision Date1993-05-18
Product CodeJAC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SOLSTICE XRAY RING MARKER PAD is the device name listed in this FDA 510(k) record. The listed applicant is Solstice Corp.. It received FDA 510(k) clearance on 1993-05-18 under 510(k) number K925892. The device is classified under product code JAC. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SOLSTICE XRAY RING MARKER PAD?

SOLSTICE XRAY RING MARKER PAD is a medical device that received FDA 510(k) clearance on 1993-05-18. The listed applicant is Solstice Corp.. The 510(k) number is K925892.

When did SOLSTICE XRAY RING MARKER PAD receive FDA 510(k) clearance?

SOLSTICE XRAY RING MARKER PAD received FDA 510(k) clearance on 1993-05-18, under 510(k) number K925892.

Who is the listed applicant for SOLSTICE XRAY RING MARKER PAD?

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

What is the FDA product code for SOLSTICE XRAY RING MARKER PAD?

The FDA product code for SOLSTICE XRAY RING MARKER PAD is JAC.

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Related Devices (Code: JAC)

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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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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