CARAPACE STERILE CAST PADDING— 510(k) K931672

Substantially Equivalent

Carapace, Inc.

FDA 510(k) clearance K931672 for CARAPACE STERILE CAST PADDING, Substantially Equivalent on 1993-12-15. Applicant: Carapace, Inc.. Device class: 1.

Clearance details

Applicant: Carapace, Inc.
Product code: Code LGF
Device class: Class 1
Regulation: 21 CFR 888.5940
Advisory panel: Orthopedic
Date received: 1993-04-06
Decision date: 1993-12-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Broken Arrow, OK, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LGF

K043526 — SILVERSEAL TUBULAR WOUND DRESSING WITH X-STATIC2005-03-10
K973417 — CLINITEX STOCKINETTE1997-12-09
K973420 — CLINITEX CAST PADDING1997-12-09
K955320 — PROTEC COTTON PADDING BANDAGE1996-01-26
K932507 — QUICK-CAST IMMOBILIZER1994-02-23

More clearances from Carapace, Inc.

K931722 — CARAPACE LABOR AND DELIVERY SETS1994-03-23
K931822 — CARAPACE PELVIC EXAM TRAYS1994-03-07
K931729 — I.V. START KIT1994-02-22
K931669 — CARAPACE DEBRIDEMENT KITS1994-02-07
K931820 — CARAPACE STILLWATER BOWL SET1994-02-07

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