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FDA 510(k)

LABSONICS MAMM-O-MATE MODEL NO. 918084-1

K-Number: K890519 · 1989-05-03

ApplicantLaboratory Equipment Corp.
Decision Date1989-05-03
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LABSONICS MAMM-O-MATE MODEL NO. 918084-1 is the device name listed in this FDA 510(k) record. The listed applicant is Laboratory Equipment Corp.. It received FDA 510(k) clearance on 1989-05-03 under 510(k) number K890519. 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 LABSONICS MAMM-O-MATE MODEL NO. 918084-1?

LABSONICS MAMM-O-MATE MODEL NO. 918084-1 is a medical device that received FDA 510(k) clearance on 1989-05-03. The listed applicant is Laboratory Equipment Corp.. The 510(k) number is K890519.

When did LABSONICS MAMM-O-MATE MODEL NO. 918084-1 receive FDA 510(k) clearance?

LABSONICS MAMM-O-MATE MODEL NO. 918084-1 received FDA 510(k) clearance on 1989-05-03, under 510(k) number K890519.

Who is the listed applicant for LABSONICS MAMM-O-MATE MODEL NO. 918084-1?

The FDA 510(k) record lists Laboratory Equipment Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LABSONICS MAMM-O-MATE MODEL NO. 918084-1?

The FDA product code for LABSONICS MAMM-O-MATE MODEL NO. 918084-1 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 Laboratory Equipment Corp. 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.

K905522LABSONICS MAMM-O-MATE MODEL NO. 918084-1, MODIFIED

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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