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510(k) K860332

DIAMOND BLADE MICROMETER KNIFE by Med-Tech Develoment Corp. — Product Code HNN

K860332 is an FDA 510(k) premarket notification submitted by Med-Tech Develoment Corp. for the device "DIAMOND BLADE MICROMETER KNIFE". The FDA issued a decision of Substantially Equivalent on February 13, 1986. The device falls under product code HNN (Knife, Ophthalmic), a Class I device regulated under 21 CFR 886.4350. Med-Tech Develoment Corp. has at least 4 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 13, 1986
Date Received
January 29, 1986
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Knife, Ophthalmic
Device Class
Class I
Regulation Number
886.4350
Review Panel
OP
Submission Type

Other clearances by Med-Tech Develoment Corp.

  • K860852 — SAPPHIRE BLADE SURGICAL KNIFE (March 28, 1986)
  • K860330 — MAKLAKOV STYLE TONOMETER (February 12, 1986)
  • K860331 — DISPOSABLE SURGICAL KNIFE (February 12, 1986)
  • K860329 — FYODOROV RADIAL KERATOTOMY MARKER SET (February 12, 1986)

Other clearances for product code HNN

  • K110166 — CLEARCUT S SAFETY KNIFE (May 20, 2011)
  • K922378 — OPHTHALMIC KNIFE (December 10, 1992)
  • K882402 — RETRACTIVE INCISION MICROMETER (RIM) GUAGE (August 22, 1988)
  • K881669 — MVR/STILETTO BLADE 20GA. - P/N 1900 (May 13, 1988)
  • K874979 — PRISMA DISPOSABLE MVR/STILETTO BLADE (April 13, 1988)
  • K874057 — OPHTHALMIC TIP & BLADE SCALPELS (December 23, 1987)
  • K874056 — OPHTHALMIC DISPOSABLE BLADES (December 22, 1987)
  • K873385 — OPHTHALMIC PHACO-BLADE (September 21, 1987)
  • K871285 — KNIFE, OPHTHALMIC (April 27, 1987)
  • K864290 — RK-M & RK-DK DIAMOND KNIVES WITH MEASURING GAUGE (December 15, 1986)

FDA data resources