FDA 510(k)

MEDSPEC RUBBER BANDS

K-Number: K800279 · 1980-05-02

Decision Date1980-05-02

Product Code

DecisionSubstantially Equivalent

Device Summary

MEDSPEC RUBBER BANDS is the device name listed in this FDA 510(k) record. The listed applicant is Medspec Corp.. It received FDA 510(k) clearance on 1980-05-02 under 510(k) number K800279. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDSPEC RUBBER BANDS?

MEDSPEC RUBBER BANDS is a medical device that received FDA 510(k) clearance on 1980-05-02. The listed applicant is Medspec Corp.. The 510(k) number is K800279.

When did MEDSPEC RUBBER BANDS receive FDA 510(k) clearance?

MEDSPEC RUBBER BANDS received FDA 510(k) clearance on 1980-05-02, under 510(k) number K800279.

Who is the listed applicant for MEDSPEC RUBBER BANDS?

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

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_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Medspec Corp. as applicant

K813012STERILE BASIN SETS K812710STERILE LAPAROTOMY SPONGES-X-RAY DETECT K812707STERILE DISSECTOR SPONGES-X-RAY DETECT K812711STERILE GAUZE PADS 12PLY K812709STERILE DENTAL ROLL K810071STERILE SILICONE TUBING

View all 15 devices →

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.