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FDA 510(k)

PALL ULTIPOR VACUUM LINE BACTERIA FITLER

K-Number: K812505 · 1981-09-16

ApplicantPall Biomedical Products Co.
Decision Date1981-09-16
Product CodeJQC
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

PALL ULTIPOR VACUUM LINE BACTERIA FITLER is the device name listed in this FDA 510(k) record. The listed applicant is Pall Biomedical Products Co.. It received FDA 510(k) clearance on 1981-09-16 under 510(k) number K812505. The device is classified under product code JQC. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PALL ULTIPOR VACUUM LINE BACTERIA FITLER?

PALL ULTIPOR VACUUM LINE BACTERIA FITLER is a medical device that received FDA 510(k) clearance on 1981-09-16. The listed applicant is Pall Biomedical Products Co.. The 510(k) number is K812505.

When did PALL ULTIPOR VACUUM LINE BACTERIA FITLER receive FDA 510(k) clearance?

PALL ULTIPOR VACUUM LINE BACTERIA FITLER received FDA 510(k) clearance on 1981-09-16, under 510(k) number K812505.

Who is the listed applicant for PALL ULTIPOR VACUUM LINE BACTERIA FITLER?

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

What is the FDA product code for PALL ULTIPOR VACUUM LINE BACTERIA FITLER?

The FDA product code for PALL ULTIPOR VACUUM LINE BACTERIA FITLER is JQC.

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Other records listing Pall Biomedical Products Co. 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.

K954331PALL LEA FILTER (LIPID EMULSION FILTER) (I.V. FILTER)K960993PALL SQ40S BLOOD FILTER (SQ40S/SQ40ST)K905794PALL 3N1 FILTERK902518LD-SIX ARTERIAL BLOOD FILTER FOR EXTRA. SERVICEK884534PALL HEPCHEK (TM) HEPARIN ABSORPTION FILTERK875095PALL CARDIOPLEGIA PLUS FILTER W/POSIDYNE MEMBRANE

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Related Devices (Code: JQC)

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.

K183205PureBMC SupraPhysiologic Concentrating System 30 mL System, PureBMC SupraPhysiologic Concentrating System 60 mL System, PureBMC SupraPhysiologic Concentrating System 120 mL SystemEmcyte CorporationK103340SMARTPREP2 BMAC SYSTEM, SMARTPREP PLATELET CONCENTRATION SYSTEMHarvest Technologies, Corp.K081345AXP PLATFORM MARROW XPRESS SYSTEM MODEL 8-5137, 8-5138, 8-5139, 8-5140 (PRIMARY)Thermogenesis Corp.K071934MARROWSTIM CONCENTRATION KIT AND MARROWSTIM MINI CONCENTRATION KITBiomet Manufacturing CorpK070666GENESISCS COMPONENT CONCENTRATING SYSTEMPerfusion Partners & Assoc., Inc.K052925SMARTPREP2 CENTRIFUGE SYSTEMHarvest Technologies, Corp.

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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