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FDA 510(k)

CARAPACE ANGIOGRAPHY TRAYS

K-Number: K931629 · 1993-12-06

ApplicantCarapace, Inc.
Decision Date1993-12-06
Product CodeDQO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CARAPACE ANGIOGRAPHY TRAYS is the device name listed in this FDA 510(k) record. The listed applicant is Carapace, Inc.. It received FDA 510(k) clearance on 1993-12-06 under 510(k) number K931629. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARAPACE ANGIOGRAPHY TRAYS?

CARAPACE ANGIOGRAPHY TRAYS is a medical device that received FDA 510(k) clearance on 1993-12-06. The listed applicant is Carapace, Inc.. The 510(k) number is K931629.

When did CARAPACE ANGIOGRAPHY TRAYS receive FDA 510(k) clearance?

CARAPACE ANGIOGRAPHY TRAYS received FDA 510(k) clearance on 1993-12-06, under 510(k) number K931629.

Who is the listed applicant for CARAPACE ANGIOGRAPHY TRAYS?

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 ANGIOGRAPHY TRAYS?

The FDA product code for CARAPACE ANGIOGRAPHY TRAYS is DQO.

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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 KITK931820CARAPACE STILLWATER BOWL SETK931669CARAPACE DEBRIDEMENT KITSK931760CARAPACE PACKING GAUZE TRAYS

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Related Devices (Code: DQO)

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.

K261455Arterial Pressure Monitoring Set/TraySpectrum VascularK252702Bioptimal Pulmonary Artery Monitoring Catheter (TD2502NF, TD2502NGF, TD2502NDF, TD2502NCF, TD2502NCGF, TD2502NDGF, TD2502NDCF, TD2502NDCGF, TD2502NXCF, TD2502NDXF, TD2502NXCGF, TD2502NDXGF, TD2502NDXCF, TD2502NDXCGF, TD2502-110NF, TD2502-110NGF, TD2502-110NDF, TD2502-110NCF, TD2502-110NDGF, TD2502-110NDCF, TD2502-110NCGF, TD2502-110NDCGF, TD2502-110NXF, TD2502-110NXGF, TD2502-110NDXF, TD2502-110NXCF, TD2502-110NDXGF, TD2502-110NDXCF ,TD2502-110NXCGF, TD2502-110NDXCGF, TD2602NF, TD2602NBioptimal International Pte. , Ltd.K254278Arterial Pressure Monitoring Set/TraySpectrum VascularK250751DualView CatheterTerumo CorporationK242966Gentuity® HF-OCT Imaging System with Vis-Rx Prime® Micro-Imaging CatheterGentuity, LLCK242420pNOVUS 21 MicrocatheterPhenox, Ltd.

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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