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FDA 510(k)

CLINITEX STOCKINETTE

K-Number: K973417 · 1997-12-09

ApplicantClinitex Medical Corp.
Decision Date1997-12-09
Product CodeLGF
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CLINITEX STOCKINETTE is the device name listed in this FDA 510(k) record. The listed applicant is Clinitex Medical Corp.. It received FDA 510(k) clearance on 1997-12-09 under 510(k) number K973417. The device is classified under product code LGF. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLINITEX STOCKINETTE?

CLINITEX STOCKINETTE is a medical device that received FDA 510(k) clearance on 1997-12-09. The listed applicant is Clinitex Medical Corp.. The 510(k) number is K973417.

When did CLINITEX STOCKINETTE receive FDA 510(k) clearance?

CLINITEX STOCKINETTE received FDA 510(k) clearance on 1997-12-09, under 510(k) number K973417.

Who is the listed applicant for CLINITEX STOCKINETTE?

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

What is the FDA product code for CLINITEX STOCKINETTE?

The FDA product code for CLINITEX STOCKINETTE is LGF.

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 Clinitex Medical Corp. 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.

K973420CLINITEX CAST PADDING

Related Devices (Code: LGF)

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.

K043526SILVERSEAL TUBULAR WOUND DRESSING WITH X-STATICNoble Fiber Technologies, Inc.K973420CLINITEX CAST PADDINGClinitex Medical Corp.K955320PROTEC COTTON PADDING BANDAGEDerivadas Degasa S.A. DE C.V.K932507QUICK-CAST IMMOBILIZERLandec Corp.K931672CARAPACE STERILE CAST PADDINGCarapace, Inc.K910274ARTIFLEX(TM)Beiersdorf, 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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