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FDA 510(k)

THE VIVACARE T.P.S. PROBE

K-Number: K944848 · 1994-12-14

ApplicantRms Div.
Decision Date1994-12-14
Product CodeEIX
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

THE VIVACARE T.P.S. PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Rms Div.. It received FDA 510(k) clearance on 1994-12-14 under 510(k) number K944848. The device is classified under product code EIX. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE VIVACARE T.P.S. PROBE?

THE VIVACARE T.P.S. PROBE is a medical device that received FDA 510(k) clearance on 1994-12-14. The listed applicant is Rms Div.. The 510(k) number is K944848.

When did THE VIVACARE T.P.S. PROBE receive FDA 510(k) clearance?

THE VIVACARE T.P.S. PROBE received FDA 510(k) clearance on 1994-12-14, under 510(k) number K944848.

Who is the listed applicant for THE VIVACARE T.P.S. PROBE?

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

What is the FDA product code for THE VIVACARE T.P.S. PROBE?

The FDA product code for THE VIVACARE T.P.S. PROBE is EIX.

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Other records listing Rms Div. 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.

K963367RMS K-WIREK954438SUNMED'S GREENLINE FIBER OPTIC LARYNGOSCOPEK944557DW250 #91K941625DW234 #29K902403ELITE R/F SPOT FILM DRIVEK902146SFD-035 SPOT FILM DEVICE

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Related Devices (Code: EIX)

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.

K960245VIP VICTOR INTERACTIVE PROBEPro-DentecK936221PROBE TIP/PERI PROBE/PERI PROBE COMP.Pd International ABK890333ALBUMIN REAGENTAlpkem Corp.K880827ACCUTEK PERIODONTAL PROBESweet Micro Systems, Inc.K875076FLORIDA PROBEFlorida Probe Corp.K870280ACCUDENT ACCUPROBEAccudent, 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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