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FDA 510(k)

DIGITAL CRADLE

K-Number: K840463 · 1984-02-21

ApplicantSpectrum X-Ray Corp.
Decision Date1984-02-21
Product CodeKXH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DIGITAL 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 1984-02-21 under 510(k) number K840463. 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 DIGITAL CRADLE?

DIGITAL CRADLE is a medical device that received FDA 510(k) clearance on 1984-02-21. The listed applicant is Spectrum X-Ray Corp.. The 510(k) number is K840463.

When did DIGITAL CRADLE receive FDA 510(k) clearance?

DIGITAL CRADLE received FDA 510(k) clearance on 1984-02-21, under 510(k) number K840463.

Who is the listed applicant for DIGITAL 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 DIGITAL CRADLE?

The FDA product code for DIGITAL 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.

K933134SPECTRUM DG-P7000 PEDIATRIC CRADLEK931563SPECTRUM MARK I SPECIAL PROCEDURES TABLEK870707PENTAMAX 1 MODEL B TABLE SYSTEMK834494SPECTRUM X-RAY CORPK827450SIMPLAMATIC IIIK813561SPECTRUM PEDIATRIC CARDLE TABLE

View all 9 devices →

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.K933134SPECTRUM DG-P7000 PEDIATRIC CRADLESpectrum X-Ray Corp.K930357ACCESSORY TO UNIVERSAL OCTOPAQUEOctostop, Inc.K884292STRETCHER TABLEFischer Imaging Corp.

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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