Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

CURITY(R) CALIB TUOHY TYPE EPIDUR NEEDLE FIX WING

K-Number: K910791 · 1991-05-17

ApplicantKendall Healthcare Products Co. Div.Of Tyco Health
Decision Date1991-05-17
Product CodeBSP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CURITY(R) CALIB TUOHY TYPE EPIDUR NEEDLE FIX WING is the device name listed in this FDA 510(k) record. The listed applicant is Kendall Healthcare Products Co. Div.Of Tyco Health. It received FDA 510(k) clearance on 1991-05-17 under 510(k) number K910791. The device is classified under product code BSP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CURITY(R) CALIB TUOHY TYPE EPIDUR NEEDLE FIX WING?

CURITY(R) CALIB TUOHY TYPE EPIDUR NEEDLE FIX WING is a medical device that received FDA 510(k) clearance on 1991-05-17. The listed applicant is Kendall Healthcare Products Co. Div.Of Tyco Health. The 510(k) number is K910791.

When did CURITY(R) CALIB TUOHY TYPE EPIDUR NEEDLE FIX WING receive FDA 510(k) clearance?

CURITY(R) CALIB TUOHY TYPE EPIDUR NEEDLE FIX WING received FDA 510(k) clearance on 1991-05-17, under 510(k) number K910791.

Who is the listed applicant for CURITY(R) CALIB TUOHY TYPE EPIDUR NEEDLE FIX WING?

The FDA 510(k) record lists Kendall Healthcare Products Co. Div.Of Tyco Health as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CURITY(R) CALIB TUOHY TYPE EPIDUR NEEDLE FIX WING?

The FDA product code for CURITY(R) CALIB TUOHY TYPE EPIDUR NEEDLE FIX WING is BSP.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Kendall Healthcare Products Co. Div.Of Tyco Health 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.

K973763KENDALL CURITY IODOFORM PACKING STRIPK973511KENDALL CURITY PETROLATUM GAUZEK973507KENDALL XEROFORM PETROLATUM DRESSING (6311,6312,6313,6314,6315,6316,6317)K973619KENDALL CURITY NON-ADHERING DRESSINGK973509KENDALL CURASORB ZN + MG ALGINATE WOUND DRESSINGK973546KENDALL FAST-CATH PRE LUBRICATED URETHRAL CATHETER

View all 66 devices →

Related Devices (Code: BSP)

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.

K243690SonoMSKPAJUNK GmbH MedizintechnologieK243682SonoPlex STIM; SonoPlex IIPAJUNK GmbH MedizintechnologieK250774SPROTTE® STANDARD (LUER/ NRFit®) Lumbar PuncturePAJUNK GmbH MedizintechnologieK243525SonoTAP and SonoTAP IIPAJUNK GmbH MedizintechnologieK241953SPROTTE® STANDARD (LUER/ NRFit®) AnesthesiologyPAJUNK GmbH MedizintechnologieK241954SonoBlock; SonoBlock IIPAJUNK GmbH Medizintechnologie

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.

↑