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FDA 510(k)

VITALMAX 4000/MINIPACK 3100/3000

K-Number: K951226 · 1996-11-21

ApplicantPace Tech, Inc.
Decision Date1996-11-21
Product CodeDSK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VITALMAX 4000/MINIPACK 3100/3000 is the device name listed in this FDA 510(k) record. The listed applicant is Pace Tech, Inc.. It received FDA 510(k) clearance on 1996-11-21 under 510(k) number K951226. The device is classified under product code DSK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VITALMAX 4000/MINIPACK 3100/3000?

VITALMAX 4000/MINIPACK 3100/3000 is a medical device that received FDA 510(k) clearance on 1996-11-21. The listed applicant is Pace Tech, Inc.. The 510(k) number is K951226.

When did VITALMAX 4000/MINIPACK 3100/3000 receive FDA 510(k) clearance?

VITALMAX 4000/MINIPACK 3100/3000 received FDA 510(k) clearance on 1996-11-21, under 510(k) number K951226.

Who is the listed applicant for VITALMAX 4000/MINIPACK 3100/3000?

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

What is the FDA product code for VITALMAX 4000/MINIPACK 3100/3000?

The FDA product code for VITALMAX 4000/MINIPACK 3100/3000 is DSK.

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Other records listing Pace Tech, Inc. 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.

K953795VITALMAX 4100K944541HANDYPACK 911SCK945385VITALMAX 800 PLUS/VITALMAX 810 PLUS/MINIPACK 300K925701MINIPACK 911-STCK934385MINIPACK 3100/3000 MODIFICATIONK933624VITALMAX 4000

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Related Devices (Code: DSK)

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.

K231586Endophys Blood Pressure Monitor model BPM-30Endophys Technologies, LLCK160945Endophys Blood Pressure MonitorEndophys Holdings, LLCK080670MODIFICATION TO SPHYGMOCOR CARDIOVASCULAR MANAGEMENT SYSTEMAtcor MedicalK070795SPHYGMOCOR CARDIOVASCULAR MANAGEMENT SYSTEMAtcor Medical Pty, Ltd.K033738MONITORING SYSTEM, MODEL ARGUS PB-2200Schiller AGK021517ABP FOR WINDOWSRozinn Electronics, 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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