LASER, CO2 SURGICAL— 510(k) K782054

Substantially Equivalent

Cavitron Corp.

FDA 510(k) clearance K782054 for LASER, CO2 SURGICAL, Substantially Equivalent on 1979-01-17. Applicant: Cavitron Corp.. Device class: 2.

Clearance details

Applicant: Cavitron Corp.
Product code: Code HHR
Device class: Class 2
Regulation: 21 CFR 884.4550
Advisory panel: Obstetrics/Gynecology
Date received: 1978-12-07
Decision date: 1979-01-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HHR

K881507 — ENDOCOAGULATOR MODEL 20 LASER & ACCESSORIES1989-04-27
K871875 — MODEL 5050 SURGILASER FOR OB-GYN USE1988-08-22
K875314 — GL-35 COLPOSCOPIC LASER SYSTEM1988-08-05
K874615 — LASER CANNISTER FILTER1988-06-23
K880591 — LASEGUIDE 600A, 600B, 400A, 400B FOR OB-GYN USE1988-06-01

More clearances from Cavitron Corp.

K811582 — THE PLACER1981-07-28
K810207 — MINOR SURGERY LIGHT1981-02-13
K802928 — SPIROMETRIC COMPUTER #SC-101980-12-17
K801623 — CAVITRON ULTRASONIC SURG. ASPIR. CUSA1980-11-18
K801877 — SLIT LAMP ATTACHMENT1980-09-16

Data sourced from openFDA. This site is unofficial and independent of the FDA.