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FDA 510(k)

KEELER LVA SYSTEM MULTI-CAP SERIES LVA51-1/2/3/4/5

K-Number: K870203 · 1987-02-12

ApplicantKeeler Instruments, Inc.
Decision Date1987-02-12
Product CodeHKK
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

KEELER LVA SYSTEM MULTI-CAP SERIES LVA51-1/2/3/4/5 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 1987-02-12 under 510(k) number K870203. The device is classified under product code HKK. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KEELER LVA SYSTEM MULTI-CAP SERIES LVA51-1/2/3/4/5?

KEELER LVA SYSTEM MULTI-CAP SERIES LVA51-1/2/3/4/5 is a medical device that received FDA 510(k) clearance on 1987-02-12. The listed applicant is Keeler Instruments, Inc.. The 510(k) number is K870203.

When did KEELER LVA SYSTEM MULTI-CAP SERIES LVA51-1/2/3/4/5 receive FDA 510(k) clearance?

KEELER LVA SYSTEM MULTI-CAP SERIES LVA51-1/2/3/4/5 received FDA 510(k) clearance on 1987-02-12, under 510(k) number K870203.

Who is the listed applicant for KEELER LVA SYSTEM MULTI-CAP SERIES LVA51-1/2/3/4/5?

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 KEELER LVA SYSTEM MULTI-CAP SERIES LVA51-1/2/3/4/5?

The FDA product code for KEELER LVA SYSTEM MULTI-CAP SERIES LVA51-1/2/3/4/5 is HKK.

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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: HKK)

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.

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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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