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FDA 510(k)

SCISSORS SHEA BELLUCC

K-Number: K833603 · 1984-01-03

ApplicantMicrotek Medical, Inc.
Decision Date1984-01-03
Product CodeJZB
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

SCISSORS SHEA BELLUCC is the device name listed in this FDA 510(k) record. The listed applicant is Microtek Medical, Inc.. It received FDA 510(k) clearance on 1984-01-03 under 510(k) number K833603. The device is classified under product code JZB. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCISSORS SHEA BELLUCC?

SCISSORS SHEA BELLUCC is a medical device that received FDA 510(k) clearance on 1984-01-03. The listed applicant is Microtek Medical, Inc.. The 510(k) number is K833603.

When did SCISSORS SHEA BELLUCC receive FDA 510(k) clearance?

SCISSORS SHEA BELLUCC received FDA 510(k) clearance on 1984-01-03, under 510(k) number K833603.

Who is the listed applicant for SCISSORS SHEA BELLUCC?

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

What is the FDA product code for SCISSORS SHEA BELLUCC?

The FDA product code for SCISSORS SHEA BELLUCC is JZB.

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Other records listing Microtek Medical, 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: JZB)

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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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