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FDA 510(k)

CARAPACE EPIDURAL BLOCK & SPINAL MYELOGRAM TRAYS

K-Number: K931670 · 1994-01-25

Decision Date1994-01-25
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CARAPACE EPIDURAL BLOCK & SPINAL MYELOGRAM 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 1994-01-25 under 510(k) number K931670. The device is classified under product code CAZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARAPACE EPIDURAL BLOCK & SPINAL MYELOGRAM TRAYS?

CARAPACE EPIDURAL BLOCK & SPINAL MYELOGRAM TRAYS is a medical device that received FDA 510(k) clearance on 1994-01-25. The listed applicant is Carapace, Inc.. The 510(k) number is K931670.

When did CARAPACE EPIDURAL BLOCK & SPINAL MYELOGRAM TRAYS receive FDA 510(k) clearance?

CARAPACE EPIDURAL BLOCK & SPINAL MYELOGRAM TRAYS received FDA 510(k) clearance on 1994-01-25, under 510(k) number K931670.

Who is the listed applicant for CARAPACE EPIDURAL BLOCK & SPINAL MYELOGRAM 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 EPIDURAL BLOCK & SPINAL MYELOGRAM TRAYS?

The FDA product code for CARAPACE EPIDURAL BLOCK & SPINAL MYELOGRAM TRAYS is CAZ.

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: CAZ)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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