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FDA 510(k)

MINI-LANCET

K-Number: K931481 · 1993-10-01

ApplicantPacific Rim Products, Inc.
Decision Date1993-10-01
Product CodeFMK
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MINI-LANCET is the device name listed in this FDA 510(k) record. The listed applicant is Pacific Rim Products, Inc.. It received FDA 510(k) clearance on 1993-10-01 under 510(k) number K931481. 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 MINI-LANCET?

MINI-LANCET is a medical device that received FDA 510(k) clearance on 1993-10-01. The listed applicant is Pacific Rim Products, Inc.. The 510(k) number is K931481.

When did MINI-LANCET receive FDA 510(k) clearance?

MINI-LANCET received FDA 510(k) clearance on 1993-10-01, under 510(k) number K931481.

Who is the listed applicant for MINI-LANCET?

The FDA 510(k) record lists Pacific Rim Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MINI-LANCET?

The FDA product code for MINI-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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