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FDA 510(k)

SILASTIC BRAND OBSTETRICAL VACUUM CUP

K-Number: K771558 · 1977-09-20

ApplicantDow Corning Corp. Healthcare Industries Materials
Decision Date1977-09-20
Product CodeHDB
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SILASTIC BRAND OBSTETRICAL VACUUM CUP is the device name listed in this FDA 510(k) record. The listed applicant is Dow Corning Corp. Healthcare Industries Materials. It received FDA 510(k) clearance on 1977-09-20 under 510(k) number K771558. The device is classified under product code HDB. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SILASTIC BRAND OBSTETRICAL VACUUM CUP?

SILASTIC BRAND OBSTETRICAL VACUUM CUP is a medical device that received FDA 510(k) clearance on 1977-09-20. The listed applicant is Dow Corning Corp. Healthcare Industries Materials. The 510(k) number is K771558.

When did SILASTIC BRAND OBSTETRICAL VACUUM CUP receive FDA 510(k) clearance?

SILASTIC BRAND OBSTETRICAL VACUUM CUP received FDA 510(k) clearance on 1977-09-20, under 510(k) number K771558.

Who is the listed applicant for SILASTIC BRAND OBSTETRICAL VACUUM CUP?

The FDA 510(k) record lists Dow Corning Corp. Healthcare Industries Materials as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SILASTIC BRAND OBSTETRICAL VACUUM CUP?

The FDA product code for SILASTIC BRAND OBSTETRICAL VACUUM CUP is HDB.

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Other records listing Dow Corning Corp. Healthcare Industries Materials 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.

K853186SILASTIC INFLATABLE BONE PLUG H.P.K844637WHITESIDE ACRYLIC CEMENT SPACER SLEEVEK850255DOW CORNING WRIGHT TITANIUM WRIST JOINT GROMMETK843995TF-II HIP PROSTHESISK842559WHITESIDE ORTHOLOC TOTAL HIP FEMORALK840357SSA HIP PROSTHESIS

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Related Devices (Code: HDB)

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.

K250298Kiwi® Complete Vacuum Delivery System, OmniCup® (VAC-DUAL M); Kiwi® Complete Vacuum Delivery System, OmniCup® with Traction Force Indicator (VAC-DUAL MT); Kiwi® Complete Vacuum Delivery System, OmniC Cup® for Cesarean Section (VAC-DUAL C); Kiwi® Complete Vacuum Delivery System, ProCup® (VAC-DUAL S)Clinical Innovations, LLCK041579MEDELA SINGLE USE SILC CUP, MODEL 077.0791Medela AGK043614VACULINK, MODEL VCL 3000Medevco, Inc.K021193FORTUNE SILICONE VACUUM SUCTION, MODEL #1300Fortune Medical Instrument Corp.K020447MITYVAC MERLIN, MODEL 10027Prism Enterprises, Inc.K013460SWIFT LOW PROFILE CUP (PRO CUP)Swift Delivery Products

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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