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FDA 510(k)

MINI LANCET-BLOOD LANCET

K-Number: K830705 · 1983-04-08

ApplicantPharmaquest Corp.
Decision Date1983-04-08
Product CodeFMA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MINI LANCET-BLOOD LANCET is the device name listed in this FDA 510(k) record. The listed applicant is Pharmaquest Corp.. It received FDA 510(k) clearance on 1983-04-08 under 510(k) number K830705. The device is classified under product code FMA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINI LANCET-BLOOD LANCET?

MINI LANCET-BLOOD LANCET is a medical device that received FDA 510(k) clearance on 1983-04-08. The listed applicant is Pharmaquest Corp.. The 510(k) number is K830705.

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

MINI LANCET-BLOOD LANCET received FDA 510(k) clearance on 1983-04-08, under 510(k) number K830705.

Who is the listed applicant for MINI LANCET-BLOOD LANCET?

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

What is the FDA product code for MINI LANCET-BLOOD LANCET?

The FDA product code for MINI LANCET-BLOOD LANCET is FMA.

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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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