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FDA 510(k)

HENSON - HAMBLIN CFS 2000 CENTRAL FIELD SCREEN

K-Number: K864467 · 1986-12-15

ApplicantKeeler Instruments, Inc.
Decision Date1986-12-15
Product CodeHOO
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

HENSON - HAMBLIN CFS 2000 CENTRAL FIELD SCREEN is the device name listed in this FDA 510(k) record. The listed applicant is Keeler Instruments, Inc.. It received FDA 510(k) clearance on 1986-12-15 under 510(k) number K864467. The device is classified under product code HOO. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HENSON - HAMBLIN CFS 2000 CENTRAL FIELD SCREEN?

HENSON - HAMBLIN CFS 2000 CENTRAL FIELD SCREEN is a medical device that received FDA 510(k) clearance on 1986-12-15. The listed applicant is Keeler Instruments, Inc.. The 510(k) number is K864467.

When did HENSON - HAMBLIN CFS 2000 CENTRAL FIELD SCREEN receive FDA 510(k) clearance?

HENSON - HAMBLIN CFS 2000 CENTRAL FIELD SCREEN received FDA 510(k) clearance on 1986-12-15, under 510(k) number K864467.

Who is the listed applicant for HENSON - HAMBLIN CFS 2000 CENTRAL FIELD SCREEN?

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

What is the FDA product code for HENSON - HAMBLIN CFS 2000 CENTRAL FIELD SCREEN?

The FDA product code for HENSON - HAMBLIN CFS 2000 CENTRAL FIELD SCREEN is HOO.

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Other records listing Keeler Instruments, 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.

K181143Keeler TonoCare TonometerK112093CRYOMATIC CRYO CONSOLE, DISPOSABLE CRYO PROBE, DISPOSABLE PROBE ADAPTERK093298PULSAIR INTELLIPUFF, PULSAIR DESKTOP MODEL 2414-P-2001, 2417-P-2000K100500PSL CLASSIC SLIT LAMPK062412CRYOMATICK060822VANTAGE INDIRECT OPHTHALMOSCOPE

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Related Devices (Code: HOO)

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.

K941723WELCH ALLYN GLAUCOMA DETECTORWelch Allyn, Inc.K930448MARCO PROJECTION PERIMETERMarco Ophthalmic, Inc.K873912RICHMOND VISUAL FIELD SCREENERRichmond Products, Inc.K860115DIGILAB CAMBRIDGE PERIMETERBio-RadK832800AUTOMATIC TANGENT SCREEN 50CooperVision, 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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