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FDA 510(k)

CARAPACE SUTURE REMOVAL TRAYS

K-Number: K931819 · 1994-01-26

ApplicantCarapace, Inc.
Decision Date1994-01-26
Product CodeIRO
Advisory CommitteePM
DecisionUnknown

Device Summary

CARAPACE SUTURE REMOVAL 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 1994-01-26 under 510(k) number K931819. The device is classified under product code IRO. It was reviewed by the PM advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the CARAPACE SUTURE REMOVAL TRAYS?

CARAPACE SUTURE REMOVAL TRAYS is a medical device that received FDA 510(k) clearance on 1994-01-26. The listed applicant is Carapace, Inc.. The 510(k) number is K931819.

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

CARAPACE SUTURE REMOVAL TRAYS received FDA 510(k) clearance on 1994-01-26, under 510(k) number K931819.

Who is the listed applicant for CARAPACE SUTURE REMOVAL 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 SUTURE REMOVAL TRAYS?

The FDA product code for CARAPACE SUTURE REMOVAL TRAYS is IRO.

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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 KITSK931820CARAPACE STILLWATER BOWL SETK931760CARAPACE PACKING GAUZE TRAYS

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Related Devices (Code: IRO)

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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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