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FDA 510(k)

MMAC II TONOMETER

K-Number: K884012 · 1989-01-06

ApplicantProfessional Technologies Corp.
Decision Date1989-01-06
Product CodeHKX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MMAC II TONOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Professional Technologies Corp.. It received FDA 510(k) clearance on 1989-01-06 under 510(k) number K884012. The device is classified under product code HKX. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MMAC II TONOMETER?

MMAC II TONOMETER is a medical device that received FDA 510(k) clearance on 1989-01-06. The listed applicant is Professional Technologies Corp.. The 510(k) number is K884012.

When did MMAC II TONOMETER receive FDA 510(k) clearance?

MMAC II TONOMETER received FDA 510(k) clearance on 1989-01-06, under 510(k) number K884012.

Who is the listed applicant for MMAC II TONOMETER?

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

What is the FDA product code for MMAC II TONOMETER?

The FDA product code for MMAC II TONOMETER is HKX.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Professional Technologies 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.

K924670DENTIN RELIEF

Related Devices (Code: HKX)

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.

K253039AUTO KERATO-REFRACTO TONOMETER TRK-3 OMNIATopcon CorporationK223739VS Tabletop TonometerMedimaging Integrated Solution, Inc.K190382Intraocular Pressure Tonometer EASYTONCompany ElamedK181260MiiS Horus Scope DPT 100Medimaging Integrated Solution, Inc (Miis)K181143Keeler TonoCare TonometerKeeler Instruments, Inc.K180820Tono Vue Non-Contact TonometerCrystalvue Medical Corporation

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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