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FDA 510(k)

BANDBAG, WRAP, STERILE

K-Number: K820692 · 1982-05-03

ApplicantContour Fabricators, Inc.
Decision Date1982-05-03
Product CodeMMP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BANDBAG, WRAP, STERILE is the device name listed in this FDA 510(k) record. The listed applicant is Contour Fabricators, Inc.. It received FDA 510(k) clearance on 1982-05-03 under 510(k) number K820692. The device is classified under product code MMP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BANDBAG, WRAP, STERILE?

BANDBAG, WRAP, STERILE is a medical device that received FDA 510(k) clearance on 1982-05-03. The listed applicant is Contour Fabricators, Inc.. The 510(k) number is K820692.

When did BANDBAG, WRAP, STERILE receive FDA 510(k) clearance?

BANDBAG, WRAP, STERILE received FDA 510(k) clearance on 1982-05-03, under 510(k) number K820692.

Who is the listed applicant for BANDBAG, WRAP, STERILE?

The FDA 510(k) record lists Contour Fabricators, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BANDBAG, WRAP, STERILE?

The FDA product code for BANDBAG, WRAP, STERILE is MMP.

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 Contour Fabricators, Inc. 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.

K090773CFI ULTRASOUND PROBE DRAPEK970900INSTRUMENT HOLDERK971040CABLE HOLDER, SUCTION TUBE HOLDERK970185STERILE DISPOSABLE EQUIPMENT MAGNET COVERK964141GE STERILE DISPOSABLE EQUIPMENT COIL COVERK963453CFI RESTRAINT BELT (CFI-168) / CFI RESTRAINT BELT (CFI-4046)

View all 8 devices →

Related Devices (Code: MMP)

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.

K091178MTP DISPOSABLE EQUIPMENT COVERS, KARL STORZ 15 TOUCH SCREENMtp Medical Technical Promotion GmbHK043234LIGHT DRAPEWrapped IN ComfortK041501GUANGZHOU FORTUNIQUE DRAPES, BAGS AND COVERSGuangzhou Fortunique , Ltd.K040794INCUBATOR CAPEWrapped IN ComfortK032065MEDLINE BAND BAGS AND EQUIPMENT COVERSMedline Industries, Inc.K023540SNAP KOVER, MODEL 01-2020; SNAP KAPS, MODEL 03-KP09Valumed

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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