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FDA 510(k)

STERILE BLOOD LANCETS

K-Number: K841677 · 1984-06-11

ApplicantAbco Dealers, Inc.
Decision Date1984-06-11
Product CodeFMK
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STERILE BLOOD LANCETS is the device name listed in this FDA 510(k) record. The listed applicant is Abco Dealers, Inc.. It received FDA 510(k) clearance on 1984-06-11 under 510(k) number K841677. 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 STERILE BLOOD LANCETS?

STERILE BLOOD LANCETS is a medical device that received FDA 510(k) clearance on 1984-06-11. The listed applicant is Abco Dealers, Inc.. The 510(k) number is K841677.

When did STERILE BLOOD LANCETS receive FDA 510(k) clearance?

STERILE BLOOD LANCETS received FDA 510(k) clearance on 1984-06-11, under 510(k) number K841677.

Who is the listed applicant for STERILE BLOOD LANCETS?

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

What is the FDA product code for STERILE BLOOD LANCETS?

The FDA product code for STERILE BLOOD LANCETS is FMK.

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Other records listing Abco Dealers, Inc. as applicant

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Related Devices (Code: FMK)

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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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