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FDA 510(k)

PROTECTOR RETRACTOR & PROTECTOR RETRACTOR WITH DRAPE

K-Number: K954824 · 1996-04-23

ApplicantMedical Creative Technologies, Inc.
Decision Date1996-04-23
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PROTECTOR RETRACTOR & PROTECTOR RETRACTOR WITH DRAPE is the device name listed in this FDA 510(k) record. The listed applicant is Medical Creative Technologies, Inc.. It received FDA 510(k) clearance on 1996-04-23 under 510(k) number K954824. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROTECTOR RETRACTOR & PROTECTOR RETRACTOR WITH DRAPE?

PROTECTOR RETRACTOR & PROTECTOR RETRACTOR WITH DRAPE is a medical device that received FDA 510(k) clearance on 1996-04-23. The listed applicant is Medical Creative Technologies, Inc.. The 510(k) number is K954824.

When did PROTECTOR RETRACTOR & PROTECTOR RETRACTOR WITH DRAPE receive FDA 510(k) clearance?

PROTECTOR RETRACTOR & PROTECTOR RETRACTOR WITH DRAPE received FDA 510(k) clearance on 1996-04-23, under 510(k) number K954824.

Who is the listed applicant for PROTECTOR RETRACTOR & PROTECTOR RETRACTOR WITH DRAPE?

The FDA 510(k) record lists Medical Creative Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PROTECTOR RETRACTOR & PROTECTOR RETRACTOR WITH DRAPE?

The FDA product code for PROTECTOR RETRACTOR & PROTECTOR RETRACTOR WITH DRAPE is KKX.

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Other records listing Medical Creative Technologies, 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.

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Related Devices (Code: KKX)

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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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