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FDA 510(k)

CARAPACE PELVIC EXAM TRAYS

K-Number: K931822 · 1994-03-07

ApplicantCarapace, Inc.
Decision Date1994-03-07
Product CodeMLT
Advisory CommitteeOB
DecisionUnknown

Device Summary

CARAPACE PELVIC EXAM 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 1994-03-07 under 510(k) number K931822. The device is classified under product code MLT. It was reviewed by the OB advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the CARAPACE PELVIC EXAM TRAYS?

CARAPACE PELVIC EXAM TRAYS is a medical device that received FDA 510(k) clearance on 1994-03-07. The listed applicant is Carapace, Inc.. The 510(k) number is K931822.

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

CARAPACE PELVIC EXAM TRAYS received FDA 510(k) clearance on 1994-03-07, under 510(k) number K931822.

Who is the listed applicant for CARAPACE PELVIC EXAM 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 PELVIC EXAM TRAYS?

The FDA product code for CARAPACE PELVIC EXAM TRAYS is MLT.

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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 SETSK931729I.V. START KITK931820CARAPACE STILLWATER BOWL SETK931669CARAPACE DEBRIDEMENT KITSK931760CARAPACE PACKING GAUZE TRAYSK932653SWISSTEK 2000(TM) CAST REMOVAL SYSTEM

View all 22 devices →

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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