SPECTRUM PEDIATRIC CARDLE TABLE
K-Number: K813561 · 1982-01-29
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Device Summary
Frequently Asked Questions
What is the SPECTRUM PEDIATRIC CARDLE TABLE?
SPECTRUM PEDIATRIC CARDLE TABLE is a medical device that received FDA 510(k) clearance on 1982-01-29. The listed applicant is Spectrum X-Ray Corp.. The 510(k) number is K813561.
When did SPECTRUM PEDIATRIC CARDLE TABLE receive FDA 510(k) clearance?
SPECTRUM PEDIATRIC CARDLE TABLE received FDA 510(k) clearance on 1982-01-29, under 510(k) number K813561.
Who is the listed applicant for SPECTRUM PEDIATRIC CARDLE TABLE?
The FDA 510(k) record lists Spectrum X-Ray Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SPECTRUM PEDIATRIC CARDLE TABLE?
The FDA product code for SPECTRUM PEDIATRIC CARDLE TABLE is KXH.
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.
Other records listing Spectrum X-Ray Corp. 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.
Related Devices (Code: KXH)
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.
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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