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FDA 510(k)

VAGI-PRESS #401

K-Number: K790851 · 1979-07-30

ApplicantC. Intl.
Decision Date1979-07-30
Product CodeKOH
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

VAGI-PRESS #401 is the device name listed in this FDA 510(k) record. The listed applicant is C. Intl.. It received FDA 510(k) clearance on 1979-07-30 under 510(k) number K790851. The device is classified under product code KOH. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VAGI-PRESS #401?

VAGI-PRESS #401 is a medical device that received FDA 510(k) clearance on 1979-07-30. The listed applicant is C. Intl.. The 510(k) number is K790851.

When did VAGI-PRESS #401 receive FDA 510(k) clearance?

VAGI-PRESS #401 received FDA 510(k) clearance on 1979-07-30, under 510(k) number K790851.

Who is the listed applicant for VAGI-PRESS #401?

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

What is the FDA product code for VAGI-PRESS #401?

The FDA product code for VAGI-PRESS #401 is KOH.

Related Clinical Trials

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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Other records listing C. Intl. 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.

K792494CATHETERIZATION FORCEPK790855SURGICAL DRAPE CLIP #201K790853EASY-SPECK790852VAGI-SPECK790854FORCEPS #101 AND #102K790856PROCTOSCOPE #501

View all 7 devices →

Related Devices (Code: KOH)

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.

K000212KSEA CHARDONNES MORCELLATION KNIFEKARL STORZ Endoscopy-America, Inc.K921730C-SECTION PACKMedikmark, Inc.K921732MINOR LAP SETMedikmark, Inc.K892693VAGINAL SPECULA: CUSCO, GUTTMAN, INFANTZinnanti Surgical Instruments, Inc.K891351NEWPORT LATERAL VAGINAL RETRACTORSimpson/Basye, Inc.K891035NEEDLE EXTENSIONSZinnanti Surgical Instruments, 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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