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FDA 510(k)

SLIT LAMP ATTACHMENT

K-Number: K801877 · 1980-09-16

ApplicantCavitron Corp.
Decision Date1980-09-16
Product CodeHQB
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SLIT LAMP ATTACHMENT is the device name listed in this FDA 510(k) record. The listed applicant is Cavitron Corp.. It received FDA 510(k) clearance on 1980-09-16 under 510(k) number K801877. The device is classified under product code HQB. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SLIT LAMP ATTACHMENT?

SLIT LAMP ATTACHMENT is a medical device that received FDA 510(k) clearance on 1980-09-16. The listed applicant is Cavitron Corp.. The 510(k) number is K801877.

When did SLIT LAMP ATTACHMENT receive FDA 510(k) clearance?

SLIT LAMP ATTACHMENT received FDA 510(k) clearance on 1980-09-16, under 510(k) number K801877.

Who is the listed applicant for SLIT LAMP ATTACHMENT?

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

What is the FDA product code for SLIT LAMP ATTACHMENT?

The FDA product code for SLIT LAMP ATTACHMENT is HQB.

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Other records listing Cavitron 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.

K811582THE PLACERK810207MINOR SURGERY LIGHTK802928SPIROMETRIC COMPUTER #SC-10K801623CAVITRON ULTRASONIC SURG. ASPIR. CUSAK800869MODEL PM-20(N)(R)CO2 PATIENT MONITOR/ALAK800722AUTO-FIELD D AUTOMATED VISUAL DETECTOR

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Related Devices (Code: HQB)

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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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