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FDA 510(k)

PROBE SHEATH FOR ADMS ULTRASOUND PROBE

K-Number: K881208 · 1988-05-16

ApplicantAdvanced Diagnostic Medical Systems, Inc.
Decision Date1988-05-16
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PROBE SHEATH FOR ADMS ULTRASOUND PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Diagnostic Medical Systems, Inc.. It received FDA 510(k) clearance on 1988-05-16 under 510(k) number K881208. 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 PROBE SHEATH FOR ADMS ULTRASOUND PROBE?

PROBE SHEATH FOR ADMS ULTRASOUND PROBE is a medical device that received FDA 510(k) clearance on 1988-05-16. The listed applicant is Advanced Diagnostic Medical Systems, Inc.. The 510(k) number is K881208.

When did PROBE SHEATH FOR ADMS ULTRASOUND PROBE receive FDA 510(k) clearance?

PROBE SHEATH FOR ADMS ULTRASOUND PROBE received FDA 510(k) clearance on 1988-05-16, under 510(k) number K881208.

Who is the listed applicant for PROBE SHEATH FOR ADMS ULTRASOUND PROBE?

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

What is the FDA product code for PROBE SHEATH FOR ADMS ULTRASOUND PROBE?

The FDA product code for PROBE SHEATH FOR ADMS ULTRASOUND PROBE is IYO.

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Other records listing Advanced Diagnostic Medical Systems, 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.

K882746ADMS SILENT NEEDLE GUNK890203ADMS BIOPSY NEEDLEK875119BIOPSY ATTACH. FOR ADMS ULTRASOUND PROBE

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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