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FDA 510(k)

SD PLUS CLINICIAN CAT# 78-8015

K-Number: K840964 · 1984-04-23

ApplicantCodman & Shurtleff, Inc.
Decision Date1984-04-23
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

SD PLUS CLINICIAN CAT# 78-8015 is the device name listed in this FDA 510(k) record. The listed applicant is Codman & Shurtleff, Inc.. It received FDA 510(k) clearance on 1984-04-23 under 510(k) number K840964. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SD PLUS CLINICIAN CAT# 78-8015?

SD PLUS CLINICIAN CAT# 78-8015 is a medical device that received FDA 510(k) clearance on 1984-04-23. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K840964.

When did SD PLUS CLINICIAN CAT# 78-8015 receive FDA 510(k) clearance?

SD PLUS CLINICIAN CAT# 78-8015 received FDA 510(k) clearance on 1984-04-23, under 510(k) number K840964.

Who is the listed applicant for SD PLUS CLINICIAN CAT# 78-8015?

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

What is the FDA product code for SD PLUS CLINICIAN CAT# 78-8015?

The FDA product code for SD PLUS CLINICIAN CAT# 78-8015 is GZJ.

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Related Devices (Code: GZJ)

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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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