MECHANICAL CYSTITOME— 510(k) K862709

Substantially Equivalent

Rudolph Beaver, Inc.

FDA 510(k) clearance K862709 for MECHANICAL CYSTITOME, Substantially Equivalent on 1986-08-01. Applicant: Rudolph Beaver, Inc.. Device class: 1.

Clearance details

Applicant: Rudolph Beaver, Inc.
Product code: Code HNY
Device class: Class 1
Regulation: 21 CFR 886.4350
Advisory panel: Ophthalmic
Date received: 1986-07-16
Decision date: 1986-08-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Waltham, MA, US

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Recent devices under product code HNY

K961524 — STERILAB CANNULAS, STERILAB CYSTOTMES, STERILAB NEEDLES AND STERILAB LENS MANIPULATORS1996-05-16
K880345 — CYSTOTOMES/KNIFES1988-05-03
K874975 — PRISMA DISPOSABLE SHARP ANGLED IRRIGAT. CYSTOTOME1988-04-13
K874976 — PRISMA DISPOS. DOUBLE SHARP IRRIGATING CYSTOTOME1988-04-13
K874983 — PRISMA DISPOSABLE ANGLED IRRIGATING CYSTOTOME1988-04-13

More clearances from Rudolph Beaver, Inc.

K883361 — ARTHRO-TRAC(TM)1988-10-13
K875030 — OCU-11988-05-03
K860305 — BEAVER MICRO-GEM GAUGE BLOCK1986-02-12
K852828 — BEAVER R-K KNIFE1985-11-04
K853129 — BEAVER MULTIPURPOSE SAPPHIRE KNIFE1985-08-06

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