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FDA 510(k)

CLINITRON C-10

K-Number: K914351 · 1992-02-14

ApplicantSsi Medical Services, Inc.
Decision Date1992-02-14
Product CodeIXQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CLINITRON C-10 is the device name listed in this FDA 510(k) record. The listed applicant is Ssi Medical Services, Inc.. It received FDA 510(k) clearance on 1992-02-14 under 510(k) number K914351. The device is classified under product code IXQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLINITRON C-10?

CLINITRON C-10 is a medical device that received FDA 510(k) clearance on 1992-02-14. The listed applicant is Ssi Medical Services, Inc.. The 510(k) number is K914351.

When did CLINITRON C-10 receive FDA 510(k) clearance?

CLINITRON C-10 received FDA 510(k) clearance on 1992-02-14, under 510(k) number K914351.

Who is the listed applicant for CLINITRON C-10?

The FDA 510(k) record lists Ssi Medical Services, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CLINITRON C-10?

The FDA product code for CLINITRON C-10 is IXQ.

Related Clinical Trials

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Other records listing Ssi Medical Services, Inc. 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.

K943385CLINITRON ELEXISK942184CLINITRON AT HOME AIR FLUIDED THERAPYK890523SUPERCAIRK882161ACUCAIR CUSHION CONTINUOUS AIRFLOW SYSTEMK863047FLEXICAIR

Related Devices (Code: IXQ)

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.

K973842CARBON FIBER CONFORMAL COUCH TOPMedtec, Inc.K960083MOVABLE CANTILEVERED RADIOGRAPHIC TABLE XRT 100, 200 & 300Wuestec Medical, Inc.K954225MED-TEC HAND GRIPMedtec, Inc.K946262EURO, SCST, SCCFT ATLAS RADIOLOGIC TABLESScott Imaging Intl., Inc.K942916OCTOPAQUE UNIVERSALOctostop, Inc.K942190ID100 MOBILE FLUOROSCOPIC EXAMINING TABLEImage Diagnostics, 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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