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FDA 510(k)

VAN DELLEN BACTERIA FILTER

K-Number: K873465 · 1988-01-20

ApplicantVan Dellen, Ltd.
Decision Date1988-01-20
Product CodeFPK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VAN DELLEN BACTERIA FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Van Dellen, Ltd.. It received FDA 510(k) clearance on 1988-01-20 under 510(k) number K873465. The device is classified under product code FPK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VAN DELLEN BACTERIA FILTER?

VAN DELLEN BACTERIA FILTER is a medical device that received FDA 510(k) clearance on 1988-01-20. The listed applicant is Van Dellen, Ltd.. The 510(k) number is K873465.

When did VAN DELLEN BACTERIA FILTER receive FDA 510(k) clearance?

VAN DELLEN BACTERIA FILTER received FDA 510(k) clearance on 1988-01-20, under 510(k) number K873465.

Who is the listed applicant for VAN DELLEN BACTERIA FILTER?

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

What is the FDA product code for VAN DELLEN BACTERIA FILTER?

The FDA product code for VAN DELLEN BACTERIA FILTER is FPK.

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Other records listing Van Dellen, Ltd. 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.

K873463VAN DELLEN ASPIRATING TUBINGK873464VAN DELLEN CANNULAK873462VAN DELLEN ASPIRATORK873164VAN DELLEN HEALON CANNULAK873162VAN DELLEN RETROBULBAR NEEDLEK873163VAN DELLEN IRRIGATING CYSTOTOME

View all 7 devices →

Related Devices (Code: FPK)

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.

K131517MEDRAD TWIST & GO HIGH PRESSURE CONNECTOR TUBINGMedrad, Inc. / Bayer Medical Care, Inc.K063114DISPOSABLE TRANSFER SETS WITH AND WITHOUT SWABBABLE VALVES AND/OR CHECK VALVESCoeur, Inc.K063239LIFESHIELD LATEX-FREE GRAVITECH FLOW CONTROLLER I.V. SETS, MODELS 17528, 17527, 17525 & 17526Hospira, Inc.K052431MEDTRONIC MINIMED LEAPFROG II INFUSION SET, MODELS MMT-801S1, MMT-801L1, MMT-801S2, MMT-801L2, MMT-803S1Medtronic MinimedK041178EMPOWER TRANSFER SET, (CAT. NO. 7725)E-Z-Em, Inc.K031808MEDRAD SWABBABLE VALVE TRANSFER SETMedrad, Inc.

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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