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FDA 510(k)

MANUAL SURGICAL INSTRUMENTS (SEVERAL MODELS)

K-Number: K884181 · 1988-11-10

ApplicantSales & Marketing Assoc.
Decision Date1988-11-10
Product CodeGEN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MANUAL SURGICAL INSTRUMENTS (SEVERAL MODELS) is the device name listed in this FDA 510(k) record. The listed applicant is Sales & Marketing Assoc.. It received FDA 510(k) clearance on 1988-11-10 under 510(k) number K884181. The device is classified under product code GEN. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MANUAL SURGICAL INSTRUMENTS (SEVERAL MODELS)?

MANUAL SURGICAL INSTRUMENTS (SEVERAL MODELS) is a medical device that received FDA 510(k) clearance on 1988-11-10. The listed applicant is Sales & Marketing Assoc.. The 510(k) number is K884181.

When did MANUAL SURGICAL INSTRUMENTS (SEVERAL MODELS) receive FDA 510(k) clearance?

MANUAL SURGICAL INSTRUMENTS (SEVERAL MODELS) received FDA 510(k) clearance on 1988-11-10, under 510(k) number K884181.

Who is the listed applicant for MANUAL SURGICAL INSTRUMENTS (SEVERAL MODELS)?

The FDA 510(k) record lists Sales & Marketing Assoc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MANUAL SURGICAL INSTRUMENTS (SEVERAL MODELS)?

The FDA product code for MANUAL SURGICAL INSTRUMENTS (SEVERAL MODELS) is GEN.

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Related Devices (Code: GEN)

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

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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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