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FDA 510(k)

PM-PAGER

K-Number: K933552 · 1994-09-22

ApplicantHill Engineering
Decision Date1994-09-22
Product CodeKMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PM-PAGER is the device name listed in this FDA 510(k) record. The listed applicant is Hill Engineering. It received FDA 510(k) clearance on 1994-09-22 under 510(k) number K933552. 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 PM-PAGER?

PM-PAGER is a medical device that received FDA 510(k) clearance on 1994-09-22. The listed applicant is Hill Engineering. The 510(k) number is K933552.

When did PM-PAGER receive FDA 510(k) clearance?

PM-PAGER received FDA 510(k) clearance on 1994-09-22, under 510(k) number K933552.

Who is the listed applicant for PM-PAGER?

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

What is the FDA product code for PM-PAGER?

The FDA product code for PM-PAGER is KMI.

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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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