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FDA 510(k)

CERULLO SUCTION REGULATOR

K-Number: K880704 · 1988-03-29

ApplicantAesculap Instruments Corp.
Decision Date1988-03-29
Product CodeGCX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CERULLO SUCTION REGULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap Instruments Corp.. It received FDA 510(k) clearance on 1988-03-29 under 510(k) number K880704. The device is classified under product code GCX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CERULLO SUCTION REGULATOR?

CERULLO SUCTION REGULATOR is a medical device that received FDA 510(k) clearance on 1988-03-29. The listed applicant is Aesculap Instruments Corp.. The 510(k) number is K880704.

When did CERULLO SUCTION REGULATOR receive FDA 510(k) clearance?

CERULLO SUCTION REGULATOR received FDA 510(k) clearance on 1988-03-29, under 510(k) number K880704.

Who is the listed applicant for CERULLO SUCTION REGULATOR?

The FDA 510(k) record lists Aesculap Instruments Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CERULLO SUCTION REGULATOR?

The FDA product code for CERULLO SUCTION REGULATOR is GCX.

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Other records listing Aesculap Instruments Corp. 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.

K885046INSITUCAT VALVE STRIPPERK890182PROTEGRAFT DV 1500, 1900 & LOW POR, UNIGRAFT DVK890443CASPAR SCALP CLIP, APPLIERK893121ROBOTRAC (TM) RETRACTOR ARMK884057ELAN-E DISPOSABLE DRAPEK860016AESCULAP BONE MILL

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Related Devices (Code: GCX)

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.

K042454STRYKER CASSETTE PUMPStryker EndoscopyK992126CIRCON SURGIFLEX WAVE TSUNAMI SUCTION-IRRIGATION SYSTEMCircon Corp.K972074SUCTION INSTRUMENTATIONWalter Lorenz Surgical, Inc.K971022CHASE SUCKERChase Medical, Inc.K964127MEDI-VAC FLEXI-CLEAR SUCTION HANDLEAllegiance Healthcare Corp.K964519CURITY THORACENTESIS TRAYKendall Healthcare Products Co. Div.Of Tyco Health

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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