DELTA-TECH(TM) CAST REMOVAL SYSTEM— 510(k) K895861

Name: FDA 510(k) clearance K895861
Creator: U.S. Food and Drug Administration
Published: 1989-10-19

Substantially Equivalent

Johnson & Johnson Professionals, Inc.

FDA 510(k) clearance K895861 for DELTA-TECH(TM) CAST REMOVAL SYSTEM, Substantially Equivalent on 1989-10-19. Applicant: Johnson & Johnson Professionals, Inc.. Device class: 1.

Clearance details

Applicant: Johnson & Johnson Professionals, Inc.
Product code: Code LGH
Device class: Class 1
Regulation: 21 CFR 888.5960
Advisory panel: Orthopedic
Date received: 1989-10-03
Decision date: 1989-10-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Raynham, MA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LGH

view all

K932653 — SWISSTEK 2000(TM) CAST REMOVAL SYSTEM1994-01-28
K901677 — CARAPACE PORTABLE CAST SAW, SWISS-EX CAST CUTTER1990-04-23
K893380 — QCR SYSTEM I AND QCR SYSTEM II1989-11-16
K873723 — PLASTER VACUUM, 230V MODEL NO. 4183-1611987-12-10
K873721 — PLASTER VACUUM, 115V MODEL NO. 4183-1601987-12-07

More clearances from Johnson & Johnson Professionals, Inc.

view all

K992173 — SIPHONGUARD CSF CONTROL DEVICE2000-04-07
K991413 — CODMAN ETHISORB DURA PATCH2000-03-13
K991222 — CODMAN MICROSENSOR VENTRICULAR CATHETER KIT1999-07-09
K982379 — SUNDT SLIM-LINE ANEURYSM CLIP APPLIER1998-12-18
K982812 — G2 TOTAL HIP SYSTEM FEMORAL STEM (11/13 TAPER)1998-12-04

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