FDA 510(k)

CARAPACE STERILE CAST PADDING

K-Number: K931672 · 1993-12-15

Decision Date1993-12-15

Product CodeLGF

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

CARAPACE STERILE CAST PADDING is the device name listed in this FDA 510(k) record. The listed applicant is Carapace, Inc.. It received FDA 510(k) clearance on 1993-12-15 under 510(k) number K931672. The device is classified under product code LGF. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARAPACE STERILE CAST PADDING?

CARAPACE STERILE CAST PADDING is a medical device that received FDA 510(k) clearance on 1993-12-15. The listed applicant is Carapace, Inc.. The 510(k) number is K931672.

When did CARAPACE STERILE CAST PADDING receive FDA 510(k) clearance?

CARAPACE STERILE CAST PADDING received FDA 510(k) clearance on 1993-12-15, under 510(k) number K931672.

Who is the listed applicant for CARAPACE STERILE CAST PADDING?

The FDA 510(k) record lists Carapace, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CARAPACE STERILE CAST PADDING?

The FDA product code for CARAPACE STERILE CAST PADDING is LGF.

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Other records listing Carapace, Inc. as applicant

K931722CARAPACE LABOR AND DELIVERY SETS K931822CARAPACE PELVIC EXAM TRAYS K931729I.V. START KIT K931669CARAPACE DEBRIDEMENT KITS K931820CARAPACE STILLWATER BOWL SET K931760CARAPACE PACKING GAUZE TRAYS

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Related Devices (Code: LGF)

K043526SILVERSEAL TUBULAR WOUND DRESSING WITH X-STATICNoble Fiber Technologies, Inc.K973417CLINITEX STOCKINETTEClinitex Medical Corp.K973420CLINITEX CAST PADDINGClinitex Medical Corp.K955320PROTEC COTTON PADDING BANDAGEDerivadas Degasa S.A. DE C.V.K932507QUICK-CAST IMMOBILIZERLandec Corp.K910274ARTIFLEX(TM)Beiersdorf, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.