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FDA 510(k)

ULTRA-FREE

K-Number: K790445 · 1979-06-28

ApplicantMillipore Corp.
Decision Date1979-06-28
Product CodeJRL
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ULTRA-FREE is the device name listed in this FDA 510(k) record. The listed applicant is Millipore Corp.. It received FDA 510(k) clearance on 1979-06-28 under 510(k) number K790445. The device is classified under product code JRL. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTRA-FREE?

ULTRA-FREE is a medical device that received FDA 510(k) clearance on 1979-06-28. The listed applicant is Millipore Corp.. The 510(k) number is K790445.

When did ULTRA-FREE receive FDA 510(k) clearance?

ULTRA-FREE received FDA 510(k) clearance on 1979-06-28, under 510(k) number K790445.

Who is the listed applicant for ULTRA-FREE?

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

What is the FDA product code for ULTRA-FREE?

The FDA product code for ULTRA-FREE is JRL.

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Other records listing Millipore Corp. 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.

K023892MILLEX VV, GV, AND HV SYRINGE FILTER UNITSK013988MILLEX GP STERILIZING FILTER UNIT, MODEL SLGP 033 RK963717MILLEX - MP FILTER UNIT (SLMPO25SS/SLMPL25SS)K941326ULTRAFREE-CLK934069MILLEX, DUALEX (PLUS, ULTRA)K924347WATERS(TM) 996 PDA

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Related Devices (Code: JRL)

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.

K822121ACRO PACKGelman Sciences, Inc.K820455CENTRIFREE MICROPARTITION SYSTEMAmicon, Inc.K820224EMIT FREELEVEL SYSTEM ISyva Co.K812750IL 703, STAT SEPARATORInstrumentation Laboratory COK813159VACUSHIELD TMGelman Sciences, Inc.K810829ACRODISCGelman Sciences, 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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