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FDA 510(k)

MODIFICATION OF PURESPERM

K-Number: K984172 · 1999-01-14

ApplicantNidacon International AB
Decision Date1999-01-14
Product CodeMQL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MODIFICATION OF PURESPERM is the device name listed in this FDA 510(k) record. The listed applicant is Nidacon International AB. It received FDA 510(k) clearance on 1999-01-14 under 510(k) number K984172. The device is classified under product code MQL. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFICATION OF PURESPERM?

MODIFICATION OF PURESPERM is a medical device that received FDA 510(k) clearance on 1999-01-14. The listed applicant is Nidacon International AB. The 510(k) number is K984172.

When did MODIFICATION OF PURESPERM receive FDA 510(k) clearance?

MODIFICATION OF PURESPERM received FDA 510(k) clearance on 1999-01-14, under 510(k) number K984172.

Who is the listed applicant for MODIFICATION OF PURESPERM?

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

What is the FDA product code for MODIFICATION OF PURESPERM?

The FDA product code for MODIFICATION OF PURESPERM is MQL.

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Other records listing Nidacon International AB as applicant

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.

K092107VITRIBLAST, THERMOBLAST, MODEL VB-010, TB-010K023206SPERM CRYOPROTECK022443SPERMASSISTK011607SPERMCATCHK012123NIDOILK011606PURESPERM BUFFER

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Related Devices (Code: MQL)

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.

K254261Vitrification Freeze Kit and Thawing Kit (CS-IVF-FK; CS-IVF-TK)CELL STORE (BEIJING) BIOTECHNOLOGY CO., LTD.K260248Ultra-Fast WarmKitazato CorporationK252672CaseBio™ Culture w/HSA (CMH5); CaseBio™ Handling w/HSA (WHH5)Casebioscience, Inc.K250445Fast Warm - NXFujifilm Irvine ScientificK251637Dewin Reproductive Media (Dewin Gamete Buffer [with HSA and without HSA]; Dewin Follicle Flushing Solution, Dewin One Step medium [with HSA and without HSA])Donnevie Medical Technology (Shanghai) Co. , Ltd.K251305Ultra-Fast Vitri; Ultra-Fast WarmKitazato Corporation

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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