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FDA 510(k)

CEILING TUBE SUPPORT CH-30X

K-Number: K920727 · 1992-04-16

ApplicantShimadzu Medical Systems
Decision Date1992-04-16
Product CodeIYB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CEILING TUBE SUPPORT CH-30X is the device name listed in this FDA 510(k) record. The listed applicant is Shimadzu Medical Systems. It received FDA 510(k) clearance on 1992-04-16 under 510(k) number K920727. The device is classified under product code IYB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CEILING TUBE SUPPORT CH-30X?

CEILING TUBE SUPPORT CH-30X is a medical device that received FDA 510(k) clearance on 1992-04-16. The listed applicant is Shimadzu Medical Systems. The 510(k) number is K920727.

When did CEILING TUBE SUPPORT CH-30X receive FDA 510(k) clearance?

CEILING TUBE SUPPORT CH-30X received FDA 510(k) clearance on 1992-04-16, under 510(k) number K920727.

Who is the listed applicant for CEILING TUBE SUPPORT CH-30X?

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

What is the FDA product code for CEILING TUBE SUPPORT CH-30X?

The FDA product code for CEILING TUBE SUPPORT CH-30X is IYB.

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Other records listing Shimadzu Medical Systems 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.

K082224DIAGNOSTIC ULTRASOUND SYSTEM SARANO, ECHO VIEW, SHIMASONICK071291ECHOVIEW / SHIMASONIC DIAGNOSTIC ULTRASOUND SYSTEM, MODEL SDU-1100K071287ECHOVIEW / SHIMASONIC DIAGNOSTIC ULTRASOUND DEVICE, MODEL SDU-2200PROK071289ECHOVIEW / SHIMASONIC DIAGNOSTIC ULTRASOUND SYSTEM, MODEL SDU-1200PROK061643ECHO VIEW/SHIMASONIC DIAGNOSTIC ULTRASOUND SYSTEM, MODEL SDU-1200PROK061637ECHOVIEW/ SHIMASONIC DIAGNOSTIC ULTRASOUND SYSTEM, MODEL SDU-2200PRO

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Related Devices (Code: IYB)

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.

K935123SUPERSTAND 300Wuestec Medical, Inc.K946261MTS-007, STS-008, SSMTS-010, EURO-40, 72, SUPER EURO 4072, 5000Scott Imaging Intl., Inc.K941004CTS SYSTEMAcoma Medical Imaging, Inc.K941017F/C/W TUBESTANDAcoma Medical Imaging, Inc.K940442MPR-814Xri, Inc.K935004MODEL ALPHA TS-2Dpa Consulting, Inc.

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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