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FDA 510(k)

SPECTRUM DG-P7000 PEDIATRIC CRADLE

K-Number: K933134 · 1993-10-07

ApplicantSpectrum X-Ray Corp.
Decision Date1993-10-07
Product CodeKXH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SPECTRUM DG-P7000 PEDIATRIC CRADLE is the device name listed in this FDA 510(k) record. The listed applicant is Spectrum X-Ray Corp.. It received FDA 510(k) clearance on 1993-10-07 under 510(k) number K933134. The device is classified under product code KXH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPECTRUM DG-P7000 PEDIATRIC CRADLE?

SPECTRUM DG-P7000 PEDIATRIC CRADLE is a medical device that received FDA 510(k) clearance on 1993-10-07. The listed applicant is Spectrum X-Ray Corp.. The 510(k) number is K933134.

When did SPECTRUM DG-P7000 PEDIATRIC CRADLE receive FDA 510(k) clearance?

SPECTRUM DG-P7000 PEDIATRIC CRADLE received FDA 510(k) clearance on 1993-10-07, under 510(k) number K933134.

Who is the listed applicant for SPECTRUM DG-P7000 PEDIATRIC CRADLE?

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 DG-P7000 PEDIATRIC CRADLE?

The FDA product code for SPECTRUM DG-P7000 PEDIATRIC CRADLE is KXH.

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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.

K931563SPECTRUM MARK I SPECIAL PROCEDURES TABLEK870707PENTAMAX 1 MODEL B TABLE SYSTEMK834494SPECTRUM X-RAY CORPK840463DIGITAL CRADLEK827450SIMPLAMATIC IIIK813561SPECTRUM PEDIATRIC CARDLE TABLE

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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.

K122174PEDIATRIC POSITIONER PAD SETGe Healthcare Coils (Usa Instruments, Inc.)K953246OCTOROLLOctostop, Inc.K930124VARIANT OF OCTOSTOP AND OCTOPAQUEOctostop, Inc.K930357ACCESSORY TO UNIVERSAL OCTOPAQUEOctostop, Inc.K884292STRETCHER TABLEFischer Imaging Corp.K863890MAMM-AIREAr Custom Medical Products, Ltd.

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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