FDA 510(k)

SITE PERISTALTIC CASSETTE

K-Number: K892911 · 1989-05-17

ApplicantSite Microsurgical Systems, Inc.

Decision Date1989-05-17

Product CodeHQC

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

SITE PERISTALTIC CASSETTE is the device name listed in this FDA 510(k) record. The listed applicant is Site Microsurgical Systems, Inc.. It received FDA 510(k) clearance on 1989-05-17 under 510(k) number K892911. The device is classified under product code HQC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SITE PERISTALTIC CASSETTE?

SITE PERISTALTIC CASSETTE is a medical device that received FDA 510(k) clearance on 1989-05-17. The listed applicant is Site Microsurgical Systems, Inc.. The 510(k) number is K892911.

When did SITE PERISTALTIC CASSETTE receive FDA 510(k) clearance?

SITE PERISTALTIC CASSETTE received FDA 510(k) clearance on 1989-05-17, under 510(k) number K892911.

Who is the listed applicant for SITE PERISTALTIC CASSETTE?

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

What is the FDA product code for SITE PERISTALTIC CASSETTE?

The FDA product code for SITE PERISTALTIC CASSETTE is HQC.

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Other records listing Site Microsurgical Systems, Inc. as applicant

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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.