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FDA 510(k)

CSPI ROTARY SURGICAL ASPIRATOR

K-Number: K841383 · 1984-03-26

ApplicantCustom Surgical Products, Inc.
Decision Date1984-03-26
Product Code
DecisionUnknown

Device Summary

CSPI ROTARY SURGICAL ASPIRATOR is the device name listed in this FDA 510(k) record. The listed applicant is Custom Surgical Products, Inc.. It received FDA 510(k) clearance on 1984-03-26 under 510(k) number K841383. FDA Decision: Unknown.

Frequently Asked Questions

What is the CSPI ROTARY SURGICAL ASPIRATOR?

CSPI ROTARY SURGICAL ASPIRATOR is a medical device that received FDA 510(k) clearance on 1984-03-26. The listed applicant is Custom Surgical Products, Inc.. The 510(k) number is K841383.

When did CSPI ROTARY SURGICAL ASPIRATOR receive FDA 510(k) clearance?

CSPI ROTARY SURGICAL ASPIRATOR received FDA 510(k) clearance on 1984-03-26, under 510(k) number K841383.

Who is the listed applicant for CSPI ROTARY SURGICAL ASPIRATOR?

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

Related Clinical Trials

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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Other records listing Custom Surgical Products, 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.

K870874CSPI SPECIMEN TRAP (NON-STERILE)K841249SUCTION CANNULASK841242CSPI PREMIUM SURGICAL ASPIRATOR

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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