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FDA 510(k)

SUN-LITE WHITE SLIT

K-Number: K840430 · 1984-05-09

ApplicantSuncoast Medical Manufacturers, Inc.
Decision Date1984-05-09
Product Code
DecisionSubstantially Equivalent

Device Summary

SUN-LITE WHITE SLIT is the device name listed in this FDA 510(k) record. The listed applicant is Suncoast Medical Manufacturers, Inc.. It received FDA 510(k) clearance on 1984-05-09 under 510(k) number K840430. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUN-LITE WHITE SLIT?

SUN-LITE WHITE SLIT is a medical device that received FDA 510(k) clearance on 1984-05-09. The listed applicant is Suncoast Medical Manufacturers, Inc.. The 510(k) number is K840430.

When did SUN-LITE WHITE SLIT receive FDA 510(k) clearance?

SUN-LITE WHITE SLIT received FDA 510(k) clearance on 1984-05-09, under 510(k) number K840430.

Who is the listed applicant for SUN-LITE WHITE SLIT?

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

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Other records listing Suncoast Medical Manufacturers, 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.

K841604ADJUST-A-TEMP HIGH TEMPERATUREK841509REPLACE-A-TIP ADJUSTABLE HIGH TEMP.K841603ADJUST-A-TEMP MICROK841459REPLACE-A-TIP ADJUST. LOW TEMP.-K841591PYRO-TIPK840376SURG-A STAT LOOP TIP

View all 31 devices →

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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