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FDA 510(k)

PRODIMED MICROINJECTION PIPETTES

K-Number: K983713 · 1999-06-08

ApplicantProdimed
Decision Date1999-06-08
Product CodeMQH
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

PRODIMED MICROINJECTION PIPETTES is the device name listed in this FDA 510(k) record. The listed applicant is Prodimed. It received FDA 510(k) clearance on 1999-06-08 under 510(k) number K983713. The device is classified under product code MQH. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRODIMED MICROINJECTION PIPETTES?

PRODIMED MICROINJECTION PIPETTES is a medical device that received FDA 510(k) clearance on 1999-06-08. The listed applicant is Prodimed. The 510(k) number is K983713.

When did PRODIMED MICROINJECTION PIPETTES receive FDA 510(k) clearance?

PRODIMED MICROINJECTION PIPETTES received FDA 510(k) clearance on 1999-06-08, under 510(k) number K983713.

Who is the listed applicant for PRODIMED MICROINJECTION PIPETTES?

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

What is the FDA product code for PRODIMED MICROINJECTION PIPETTES?

The FDA product code for PRODIMED MICROINJECTION PIPETTES is MQH.

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Related Devices (Code: MQH)

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.

K250838Denudation PipettesGuangzhou Pinzhi Medical Device Co., Ltd.K192146V-DENUPETVitromed GmbHK161275EZ-Tip Singles, EZ-Tip Vial of 20, EZ-GripResearch Instruments LimitedK152581LifeGlobal Micro TipsLife Global Group, LLCK151018Embryo Biopsy Pipette, Polar Body Biopsy Pipette, Testicular Sperm Extraction PipetteCook IncorporatedK102480INJECTION PIPETTE; HOLDING PIPETTE; BIOPSY PIPETTE; DENUDING PIPETTE; PARTIAL ZONA DISSECTION (PZD) PIPETTE; ASSISTED HAJieying Laboratory, Inc.

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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