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)

SURGI-SCRAPE

K-Number: K820443 · 1982-03-08

ApplicantConsolidated Medical Equipment, Inc.
Decision Date1982-03-08
Product Code
DecisionSubstantially Equivalent

Device Summary

SURGI-SCRAPE is the device name listed in this FDA 510(k) record. The listed applicant is Consolidated Medical Equipment, Inc.. It received FDA 510(k) clearance on 1982-03-08 under 510(k) number K820443. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGI-SCRAPE?

SURGI-SCRAPE is a medical device that received FDA 510(k) clearance on 1982-03-08. The listed applicant is Consolidated Medical Equipment, Inc.. The 510(k) number is K820443.

When did SURGI-SCRAPE receive FDA 510(k) clearance?

SURGI-SCRAPE received FDA 510(k) clearance on 1982-03-08, under 510(k) number K820443.

Who is the listed applicant for SURGI-SCRAPE?

The FDA 510(k) record lists Consolidated Medical Equipment, Inc. 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_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 Consolidated Medical Equipment, 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.

K854040I.V. DRESSINGK850130PRN ECG ELECTRODEK850132DISPOSABLE CONDUCTIVE ADHESIVE DIAGNOSTIC ECG ELECK850037CLOSED WOUND DRAINK844942PLURA-GARD CHEST DRAINAGE SYSTEMK850131CONDUCTIVE ADHESIVE POST-OP ELECTRODE-TENS

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.

↑