CARAPACE LABOR AND DELIVERY SETS
K-Number: K931722 · 1994-03-23
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Device Summary
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.
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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