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FDA 510(k)

CARAPACE STILLWATER BOWL SET

K-Number: K931820 · 1994-02-07

ApplicantCarapace, Inc.
Decision Date1994-02-07
Product CodeLRO
Advisory CommitteeSU
DecisionUnknown

Device Summary

CARAPACE STILLWATER BOWL SET is the device name listed in this FDA 510(k) record. The listed applicant is Carapace, Inc.. It received FDA 510(k) clearance on 1994-02-07 under 510(k) number K931820. The device is classified under product code LRO. It was reviewed by the SU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the CARAPACE STILLWATER BOWL SET?

CARAPACE STILLWATER BOWL SET is a medical device that received FDA 510(k) clearance on 1994-02-07. The listed applicant is Carapace, Inc.. The 510(k) number is K931820.

When did CARAPACE STILLWATER BOWL SET receive FDA 510(k) clearance?

CARAPACE STILLWATER BOWL SET received FDA 510(k) clearance on 1994-02-07, under 510(k) number K931820.

Who is the listed applicant for CARAPACE STILLWATER BOWL SET?

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 STILLWATER BOWL SET?

The FDA product code for CARAPACE STILLWATER BOWL SET is LRO.

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Other records listing Carapace, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K931722CARAPACE LABOR AND DELIVERY SETSK931822CARAPACE PELVIC EXAM TRAYSK931729I.V. START KITK931669CARAPACE DEBRIDEMENT KITSK931760CARAPACE PACKING GAUZE TRAYSK932653SWISSTEK 2000(TM) CAST REMOVAL SYSTEM

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Related Devices (Code: LRO)

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K213481Medline General Surgery TrayMedline Industries, Inc.K212258Medline Cardiovascular Procedure KitMedline Industries, Inc.K041080SURGICAL DRAPE KIT - D.I.R.R.A. SRLD.I.R.R.A. S.R.L.K030721QUICK-TAP PARACENTESIS TRAY, KIT & NEEDLEBallard Medical ProductsK023276AMSINO TRACHEOSTOMY CARE TRAYAmsino International, Inc.K980137WORLDWIDE MEDICAL TECHNOLOGIES BONE MARROW BIOPSY PROCEDURE TRAYWorldwide Medical Technologies, LLC

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.

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