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FDA 510(k)

BLOOD LANCET

K-Number: K865016 · 1987-01-12

ApplicantFalcon Medical Industries, Inc.
Decision Date1987-01-12
Product CodeFMK
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BLOOD LANCET is the device name listed in this FDA 510(k) record. The listed applicant is Falcon Medical Industries, Inc.. It received FDA 510(k) clearance on 1987-01-12 under 510(k) number K865016. 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 BLOOD LANCET?

BLOOD LANCET is a medical device that received FDA 510(k) clearance on 1987-01-12. The listed applicant is Falcon Medical Industries, Inc.. The 510(k) number is K865016.

When did BLOOD LANCET receive FDA 510(k) clearance?

BLOOD LANCET received FDA 510(k) clearance on 1987-01-12, under 510(k) number K865016.

Who is the listed applicant for BLOOD LANCET?

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

What is the FDA product code for BLOOD LANCET?

The FDA product code for BLOOD LANCET is FMK.

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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

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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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