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FDA 510(k)

AMG + MED LANCET

K-Number: K870017 · 1987-01-21

ApplicantCan-Am Surgical Corp.
Decision Date1987-01-21
Product CodeFMK
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

AMG + MED LANCET is the device name listed in this FDA 510(k) record. The listed applicant is Can-Am Surgical Corp.. It received FDA 510(k) clearance on 1987-01-21 under 510(k) number K870017. The device is classified under product code FMK. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMG + MED LANCET?

AMG + MED LANCET is a medical device that received FDA 510(k) clearance on 1987-01-21. The listed applicant is Can-Am Surgical Corp.. The 510(k) number is K870017.

When did AMG + MED LANCET receive FDA 510(k) clearance?

AMG + MED LANCET received FDA 510(k) clearance on 1987-01-21, under 510(k) number K870017.

Who is the listed applicant for AMG + MED LANCET?

The FDA 510(k) record lists Can-Am Surgical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AMG + MED LANCET?

The FDA product code for AMG + MED LANCET is FMK.

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 Can-Am Surgical 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.

K870192DISPOSABLE SYRINGE TUBERCULIN W/NEEDLEK870190DISPOSABLE SYRINGE W/O NEEDLEK870191DISPOSABLE SYRINGE WITH NEEDLEK870193A+MED DISPOSABLE NEEDLEK870018E-Z JECT INSULIN SYRINGE

Related Devices (Code: FMK)

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.

K262526Safety lancet (XL)Tianjin Huahong Technology Co., Ltd.K261045Verifine Safety LancetsPromisemed Hangzhou Meditech Co., Ltd.K260191Safety lancet (XXXVII)Tianjin Huahong Technology Co., Ltd.K253605Safety Heel LancetNingbo Medsun Medical Co., Ltd.K252490Heel Stick Safety Lancet (HHZ-II, HHZ-III, HHZ-IV)Tianjin Huahong Technology Co., Ltd.K251694safety lancetTianjin Huahong Technology Co., Ltd.

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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