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)

PDI SURGICAL SCRUB/BRUSH T150-70

K-Number: K833549 · 1983-11-28

ApplicantNice-Pak Products, Inc.
Decision Date1983-11-28
Product CodeNAB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PDI SURGICAL SCRUB/BRUSH T150-70 is the device name listed in this FDA 510(k) record. The listed applicant is Nice-Pak Products, Inc.. It received FDA 510(k) clearance on 1983-11-28 under 510(k) number K833549. The device is classified under product code NAB. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PDI SURGICAL SCRUB/BRUSH T150-70?

PDI SURGICAL SCRUB/BRUSH T150-70 is a medical device that received FDA 510(k) clearance on 1983-11-28. The listed applicant is Nice-Pak Products, Inc.. The 510(k) number is K833549.

When did PDI SURGICAL SCRUB/BRUSH T150-70 receive FDA 510(k) clearance?

PDI SURGICAL SCRUB/BRUSH T150-70 received FDA 510(k) clearance on 1983-11-28, under 510(k) number K833549.

Who is the listed applicant for PDI SURGICAL SCRUB/BRUSH T150-70?

The FDA 510(k) record lists Nice-Pak Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PDI SURGICAL SCRUB/BRUSH T150-70?

The FDA product code for PDI SURGICAL SCRUB/BRUSH T150-70 is NAB.

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 Nice-Pak Products, 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.

K974768PDI STERILE LUBRICATING JELLYK840343PDI PREPMASTER WET PACK VAGINAL-X21477K840342PDI PREPMASTER WET PACK PATIENT PREP KITK840344PDI PREPMASTER WET PACK MINOR PROCEDUREK810337PDI SURGICAL SCRUB SPONGE-BRUSH-T15070K781539ISO-CARE KIT

View all 9 devices →

Related Devices (Code: NAB)

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.

K946015IVALON EXTERNAL SPONGEIvalonK940755ISOLYER (4X4, 8PLY)Isolyer Co.K931610OMNISORB II, NONWOVEN SPONGE, STERILE AND NONOmni Mfg., Inc.K925590MULTI-TRAUMA DRESSINGGam Industries, Inc.K926072K-BAND AND K-CREPEParema , Ltd.K915591STERILE GAUZE PADSEagle Medical, 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.

↑