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FDA 510(k)

MODIFIED SCHNEIDER-SHILEY PRESSURE MANOMETER

K-Number: K875322 · 1988-03-28

ApplicantSchneider-Shilley (Usa)
Decision Date1988-03-28
Product CodeKRK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODIFIED SCHNEIDER-SHILEY PRESSURE MANOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Schneider-Shilley (Usa). It received FDA 510(k) clearance on 1988-03-28 under 510(k) number K875322. The device is classified under product code KRK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED SCHNEIDER-SHILEY PRESSURE MANOMETER?

MODIFIED SCHNEIDER-SHILEY PRESSURE MANOMETER is a medical device that received FDA 510(k) clearance on 1988-03-28. The listed applicant is Schneider-Shilley (Usa). The 510(k) number is K875322.

When did MODIFIED SCHNEIDER-SHILEY PRESSURE MANOMETER receive FDA 510(k) clearance?

MODIFIED SCHNEIDER-SHILEY PRESSURE MANOMETER received FDA 510(k) clearance on 1988-03-28, under 510(k) number K875322.

Who is the listed applicant for MODIFIED SCHNEIDER-SHILEY PRESSURE MANOMETER?

The FDA 510(k) record lists Schneider-Shilley (Usa) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODIFIED SCHNEIDER-SHILEY PRESSURE MANOMETER?

The FDA product code for MODIFIED SCHNEIDER-SHILEY PRESSURE MANOMETER is KRK.

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Other records listing Schneider-Shilley (Usa) 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.

K882826SOFTRAC-PTA PERIPHERAL DILATATION CATHETERK875175MODIFIED PERIPHERAL DILATATION CATHETERSK881197SOFTRAC-PTA(TM) PERIPHERAL DILATATION CATHETERK875323MODIFIED SCHNEIDER-SHILEY WIRE TORQUERK875327MODIFIED SELDINGER INITIAL PUNCTURE INSTRUMENTK875324MODIFIED SCHNEIDER SHILEY INFLATION SYRINGES

View all 9 devices →

Related Devices (Code: KRK)

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.

K950607UST-5268P-5 TRANSDUCERAloka Co., Ltd.K904674CENTRAL VENOUS PRESSURE MANOMETERMedex, Inc.K884386ADMINISTRATION/MANOMETER SET W/3 WAY STOPCOCKEthitek Pharmaceuticals Co.K861605SCHNEIDER-SHILEY PRESSURE MANOMETERShiley, Inc.K830910MANOMETER SET C.V.P. #S 298/299Exco, Inc.K813498MEDIFIXBurron Medical Products, Inc.

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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