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FDA 510(k)

SPIRIT II AND SPIRIT TREATMENT CENTER

K-Number: K946187 · 1995-03-01

ApplicantPelton & Crane Co.
Decision Date1995-03-01
Product CodeEIA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SPIRIT II AND SPIRIT TREATMENT CENTER is the device name listed in this FDA 510(k) record. The listed applicant is Pelton & Crane Co.. It received FDA 510(k) clearance on 1995-03-01 under 510(k) number K946187. The device is classified under product code EIA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPIRIT II AND SPIRIT TREATMENT CENTER?

SPIRIT II AND SPIRIT TREATMENT CENTER is a medical device that received FDA 510(k) clearance on 1995-03-01. The listed applicant is Pelton & Crane Co.. The 510(k) number is K946187.

When did SPIRIT II AND SPIRIT TREATMENT CENTER receive FDA 510(k) clearance?

SPIRIT II AND SPIRIT TREATMENT CENTER received FDA 510(k) clearance on 1995-03-01, under 510(k) number K946187.

Who is the listed applicant for SPIRIT II AND SPIRIT TREATMENT CENTER?

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

What is the FDA product code for SPIRIT II AND SPIRIT TREATMENT CENTER?

The FDA product code for SPIRIT II AND SPIRIT TREATMENT CENTER is EIA.

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Other records listing Pelton & Crane 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.

K972249ORTHOPHOS PLUS AND ORTHOPHOS PLUS/CDK972168SIDEXIS DIGITAL RADIOGRAPHY SYSTEMK945117DELTAK962071SPIRIT S1/S2K960819HELIODENT DSK950299CEREC 2

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Related Devices (Code: EIA)

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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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