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FDA 510(k)

OBF MODEL 112 VACUUM CUP SYSTEM

K-Number: K864959 · 1987-02-12

ApplicantOcular Blood Flow Laboratories, Inc.
Decision Date1987-02-12
Product CodeHKX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

OBF MODEL 112 VACUUM CUP SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Ocular Blood Flow Laboratories, Inc.. It received FDA 510(k) clearance on 1987-02-12 under 510(k) number K864959. 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 OBF MODEL 112 VACUUM CUP SYSTEM?

OBF MODEL 112 VACUUM CUP SYSTEM is a medical device that received FDA 510(k) clearance on 1987-02-12. The listed applicant is Ocular Blood Flow Laboratories, Inc.. The 510(k) number is K864959.

When did OBF MODEL 112 VACUUM CUP SYSTEM receive FDA 510(k) clearance?

OBF MODEL 112 VACUUM CUP SYSTEM received FDA 510(k) clearance on 1987-02-12, under 510(k) number K864959.

Who is the listed applicant for OBF MODEL 112 VACUUM CUP SYSTEM?

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

What is the FDA product code for OBF MODEL 112 VACUUM CUP SYSTEM?

The FDA product code for OBF MODEL 112 VACUUM CUP SYSTEM is HKX.

Related Clinical Trials

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Other records listing Ocular Blood Flow Laboratories, 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.

K873422OBF MODEL 115 COMPUTER TONOMETER SYSTEM

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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