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FDA 510(k)

RSVP RF-2000

K-Number: K905586 · 1991-04-01

ApplicantTactilitics, Inc.
Decision Date1991-04-01
Product CodeKMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

RSVP RF-2000 is the device name listed in this FDA 510(k) record. The listed applicant is Tactilitics, Inc.. It received FDA 510(k) clearance on 1991-04-01 under 510(k) number K905586. The device is classified under product code KMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RSVP RF-2000?

RSVP RF-2000 is a medical device that received FDA 510(k) clearance on 1991-04-01. The listed applicant is Tactilitics, Inc.. The 510(k) number is K905586.

When did RSVP RF-2000 receive FDA 510(k) clearance?

RSVP RF-2000 received FDA 510(k) clearance on 1991-04-01, under 510(k) number K905586.

Who is the listed applicant for RSVP RF-2000?

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

What is the FDA product code for RSVP RF-2000?

The FDA product code for RSVP RF-2000 is KMI.

Other records listing Tactilitics, 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.

K864827RSVP SYSTEMS, SERIES I, BED-PATIENT MONITOR

Related Devices (Code: KMI)

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.

K131585INTEL-GE CARE INNOVATIONS QUIETCAREIntel-Ge Care Innovations, LLCK130752DYNASENSE SYSTEMCentauri Medical, Inc.K101109VIVATRAKWireless Medcare, LLCK090138MOBILECARE MONITOR, MODEL 2100Aframe Digital, Inc.K942770ULTIMAT-SENSOR FOR BED OCCUPANCY MONITORUltimate Development Corp.K943481INFORMER PLUSMicro-Tech Medical, 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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