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FDA 510(k)

SUPRAPUBIC TROCAR

K-Number: K800607 · 1980-04-08

ApplicantG.D. Searle and Co.
Decision Date1980-04-08
Product CodeKOB
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SUPRAPUBIC TROCAR is the device name listed in this FDA 510(k) record. The listed applicant is G.D. Searle and Co.. It received FDA 510(k) clearance on 1980-04-08 under 510(k) number K800607. The device is classified under product code KOB. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUPRAPUBIC TROCAR?

SUPRAPUBIC TROCAR is a medical device that received FDA 510(k) clearance on 1980-04-08. The listed applicant is G.D. Searle and Co.. The 510(k) number is K800607.

When did SUPRAPUBIC TROCAR receive FDA 510(k) clearance?

SUPRAPUBIC TROCAR received FDA 510(k) clearance on 1980-04-08, under 510(k) number K800607.

Who is the listed applicant for SUPRAPUBIC TROCAR?

The FDA 510(k) record lists G.D. Searle and Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUPRAPUBIC TROCAR?

The FDA product code for SUPRAPUBIC TROCAR is KOB.

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Other records listing G.D. Searle and Co. as applicant

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Related Devices (Code: KOB)

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.

K240514AMT Low-Profile Suprapubic Catheter & Drainage SetApplied Medical Technology, Inc.K181097Cook Cystostomy Catheter SetCook IncorporatedK182709One-Step Suprapubic IntroducerCook IncorporatedK182066O'Brien Suprapubic Introducer Set, Cook SP Tube Introducer SetCook IncorporatedK120127SWAN VALLEY MEDICAL TRANURETHRAL SUPRAPUBIC ENDO-CYSTOSTOMY (T-SPEC) SURGICAL SYSTEMSwan Valley Medical, IncorporatedK014002ALL SILICONE SUPRA-PUBIA CATHETER, MODELS 4880/4890Fortune Medical Instrument Corp.

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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