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FDA 510(k)

COMBISON(R) 310A REAL TIME ULTRASOUND SCANNER

K-Number: K873159 · 1988-03-01

ApplicantCone Instruments, Inc.
Decision Date1988-03-01
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

COMBISON(R) 310A REAL TIME ULTRASOUND SCANNER is the device name listed in this FDA 510(k) record. The listed applicant is Cone Instruments, Inc.. It received FDA 510(k) clearance on 1988-03-01 under 510(k) number K873159. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMBISON(R) 310A REAL TIME ULTRASOUND SCANNER?

COMBISON(R) 310A REAL TIME ULTRASOUND SCANNER is a medical device that received FDA 510(k) clearance on 1988-03-01. The listed applicant is Cone Instruments, Inc.. The 510(k) number is K873159.

When did COMBISON(R) 310A REAL TIME ULTRASOUND SCANNER receive FDA 510(k) clearance?

COMBISON(R) 310A REAL TIME ULTRASOUND SCANNER received FDA 510(k) clearance on 1988-03-01, under 510(k) number K873159.

Who is the listed applicant for COMBISON(R) 310A REAL TIME ULTRASOUND SCANNER?

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

What is the FDA product code for COMBISON(R) 310A REAL TIME ULTRASOUND SCANNER?

The FDA product code for COMBISON(R) 310A REAL TIME ULTRASOUND SCANNER is IYO.

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Other records listing Cone Instruments, 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.

K960665ECHO-COM FOR MS-WINDOWS VERSION 2.0K861376COMBISON R 320AK832501ENEMA TUBE

Related Devices (Code: IYO)

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.

K260313MD-6000S Bladder ScannerMEDA Co., Ltd.K253452Accuro 3SRivanna Medical, Inc.K260190ARTHURROPCA ApSK252237EdgeFlow UW20Edgecare, Inc.K254021Accuro XVRivanna Medical, Inc.K253898QT Scanner 2000 Model AQT Imaging Holdings, 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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