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510(k) K860329

FYODOROV RADIAL KERATOTOMY MARKER SET by Med-Tech Develoment Corp. — Product Code HHR

K860329 is an FDA 510(k) premarket notification submitted by Med-Tech Develoment Corp. for the device "FYODOROV RADIAL KERATOTOMY MARKER SET". The FDA issued a decision of Substantially Equivalent on February 12, 1986. The device falls under product code HHR (Laser, Surgical, Gynecologic), a Class II device regulated under 21 CFR 884.4550. Med-Tech Develoment Corp. has at least 4 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 12, 1986
Date Received
January 29, 1986
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Laser, Surgical, Gynecologic
Device Class
Class II
Regulation Number
884.4550
Review Panel
OB
Submission Type

Other clearances by Med-Tech Develoment Corp.

  • K860852 — SAPPHIRE BLADE SURGICAL KNIFE (March 28, 1986)
  • K860332 — DIAMOND BLADE MICROMETER KNIFE (February 13, 1986)
  • K860330 — MAKLAKOV STYLE TONOMETER (February 12, 1986)
  • K860331 — DISPOSABLE SURGICAL KNIFE (February 12, 1986)

Other clearances for product code HHR

  • K881507 — ENDOCOAGULATOR MODEL 20 LASER & ACCESSORIES (April 27, 1989)
  • K871875 — MODEL 5050 SURGILASER FOR OB-GYN USE (August 22, 1988)
  • K875314 — GL-35 COLPOSCOPIC LASER SYSTEM (August 5, 1988)
  • K874615 — LASER CANNISTER FILTER (June 23, 1988)
  • K880591 — LASEGUIDE 600A, 600B, 400A, 400B FOR OB-GYN USE (June 1, 1988)
  • K880930 — MDLS 4000,4900,6000,8000,8900 ND:YAG/1700 C02 LASE (May 31, 1988)
  • K880991 — LASER OPTICAL CATHETER SYSTEM (May 25, 1988)
  • K880173 — MODEL 4900 ND:YAG LASER FOR ENDOMETRIAL ABLATION (March 24, 1988)
  • K874837 — KTP/532 LASER FOR OB-GYN USE (March 14, 1988)
  • K875078 — HERACURE LS 500 (February 22, 1988)

FDA data resources