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FDA 510(k)

MODIFIED SITE PERISTALTIC FOOTSWITCH

K-Number: K905620 · 1991-02-27

ApplicantSite Microsurgical Systems, Inc.
Decision Date1991-02-27
Product CodeEBW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MODIFIED SITE PERISTALTIC FOOTSWITCH 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 1991-02-27 under 510(k) number K905620. The device is classified under product code EBW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED SITE PERISTALTIC FOOTSWITCH?

MODIFIED SITE PERISTALTIC FOOTSWITCH is a medical device that received FDA 510(k) clearance on 1991-02-27. The listed applicant is Site Microsurgical Systems, Inc.. The 510(k) number is K905620.

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

MODIFIED SITE PERISTALTIC FOOTSWITCH received FDA 510(k) clearance on 1991-02-27, under 510(k) number K905620.

Who is the listed applicant for MODIFIED SITE PERISTALTIC FOOTSWITCH?

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 MODIFIED SITE PERISTALTIC FOOTSWITCH?

The FDA product code for MODIFIED SITE PERISTALTIC FOOTSWITCH is EBW.

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Other records listing Site Microsurgical Systems, 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.

K925828MODIFIED SITE TXR SYSTEMSK925921MODIFIED SITE DISPOSABLE DIAPHRAGM CASSETTEK931866SITE'S CD II PHACOEMULSIFICATION HANDPIECEK921135IOLAB POWER I.V. POLEK920582180 TIP, 1/A HANDPIECE .3MM END OPENING FOR OPHT.K912902PHACOEMULSIFICATION SYSTEM FOR OPHTHALMIC USE

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Related Devices (Code: EBW)

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

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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