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FDA 510(k)

CARAPACE LABOR AND DELIVERY SETS

K-Number: K931722 · 1994-03-23

Decision Date1994-03-23
Product CodeMLS
Advisory CommitteeOB
DecisionUnknown

Device Summary

CARAPACE LABOR AND DELIVERY SETS is the device name listed in this FDA 510(k) record. The listed applicant is Carapace, Inc.. It received FDA 510(k) clearance on 1994-03-23 under 510(k) number K931722. The device is classified under product code MLS. It was reviewed by the OB advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the CARAPACE LABOR AND DELIVERY SETS?

CARAPACE LABOR AND DELIVERY SETS is a medical device that received FDA 510(k) clearance on 1994-03-23. The listed applicant is Carapace, Inc.. The 510(k) number is K931722.

When did CARAPACE LABOR AND DELIVERY SETS receive FDA 510(k) clearance?

CARAPACE LABOR AND DELIVERY SETS received FDA 510(k) clearance on 1994-03-23, under 510(k) number K931722.

Who is the listed applicant for CARAPACE LABOR AND DELIVERY SETS?

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 LABOR AND DELIVERY SETS?

The FDA product code for CARAPACE LABOR AND DELIVERY SETS is MLS.

Related Clinical Trials

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.

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.

View all 22 devices →

Related Devices (Code: MLS)

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.

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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