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FDA 510(k)

E-PACK PROCEDURE KITS

K-Number: K951476 · 1995-05-23

ApplicantETHICON, Inc.
Decision Date1995-05-23
Product CodeMCY
Advisory CommitteeHO
DecisionUnknown

Device Summary

E-PACK PROCEDURE KITS is the device name listed in this FDA 510(k) record. The listed applicant is ETHICON, Inc.. It received FDA 510(k) clearance on 1995-05-23 under 510(k) number K951476. The device is classified under product code MCY. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the E-PACK PROCEDURE KITS?

E-PACK PROCEDURE KITS is a medical device that received FDA 510(k) clearance on 1995-05-23. The listed applicant is ETHICON, Inc.. The 510(k) number is K951476.

When did E-PACK PROCEDURE KITS receive FDA 510(k) clearance?

E-PACK PROCEDURE KITS received FDA 510(k) clearance on 1995-05-23, under 510(k) number K951476.

Who is the listed applicant for E-PACK PROCEDURE KITS?

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

What is the FDA product code for E-PACK PROCEDURE KITS?

The FDA product code for E-PACK PROCEDURE KITS is MCY.

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Related Devices (Code: MCY)

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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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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