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)

CLEAR-VIEW MIRROR WARMER

K-Number: K800382 · 1980-05-14

ApplicantSurgical Mechanical Research, Inc.
Decision Date1980-05-14
Product CodeGET
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CLEAR-VIEW MIRROR WARMER is the device name listed in this FDA 510(k) record. The listed applicant is Surgical Mechanical Research, Inc.. It received FDA 510(k) clearance on 1980-05-14 under 510(k) number K800382. The device is classified under product code GET. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLEAR-VIEW MIRROR WARMER?

CLEAR-VIEW MIRROR WARMER is a medical device that received FDA 510(k) clearance on 1980-05-14. The listed applicant is Surgical Mechanical Research, Inc.. The 510(k) number is K800382.

When did CLEAR-VIEW MIRROR WARMER receive FDA 510(k) clearance?

CLEAR-VIEW MIRROR WARMER received FDA 510(k) clearance on 1980-05-14, under 510(k) number K800382.

Who is the listed applicant for CLEAR-VIEW MIRROR WARMER?

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

What is the FDA product code for CLEAR-VIEW MIRROR WARMER?

The FDA product code for CLEAR-VIEW MIRROR WARMER is GET.

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 Surgical Mechanical Research, 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.

K803195SYSTEM 1 INSTRUMENT STANDK800526SMR H-CHAIRK781801MAXI-CHAIR

Related Devices (Code: GET)

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.

K960473AESCULAP POWER SYSTEM HANDPIECEAesculap, Inc.K955174SODEM HIGH SPEED SYSTEM FOR NEUROSURGERY & MEDIAN STYERNOTOMYSodem Diffusion SAK942987NUCLEOTOME L KITSurgical Dynamics, Inc.K954076MIDAS REX DRILL ATTACHMENTS & TWIST DRILLSMidas Rex Pneumatic Tools, Inc.K953433MIDAS REX TELESCOPING SYSTEMMidas Rex Pneumatic Tools, Inc.K953432ROTATING, FIXED FOOTED, FIXED SHIELD ATTACHMENTS, DISSECTING TOOLSMidas Rex Pneumatic Tools, 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.

↑