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FDA 510(k)

COMBISON R 320A

K-Number: K861376 · 1986-07-03

ApplicantCone Instruments, Inc.
Decision Date1986-07-03
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

COMBISON R 320A 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 1986-07-03 under 510(k) number K861376. 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 320A?

COMBISON R 320A is a medical device that received FDA 510(k) clearance on 1986-07-03. The listed applicant is Cone Instruments, Inc.. The 510(k) number is K861376.

When did COMBISON R 320A receive FDA 510(k) clearance?

COMBISON R 320A received FDA 510(k) clearance on 1986-07-03, under 510(k) number K861376.

Who is the listed applicant for COMBISON R 320A?

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 320A?

The FDA product code for COMBISON R 320A is IYO.

Related Clinical Trials

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.

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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 2.0K873159COMBISON(R) 310A REAL TIME ULTRASOUND SCANNERK832501ENEMA 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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