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FDA 510(k)

G.R.A.M. SLIDE

K-Number: K802509 · 1980-11-12

ApplicantSterilization Technical Services, Inc.
Decision Date1980-11-12
Product CodeJTO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

G.R.A.M. SLIDE is the device name listed in this FDA 510(k) record. The listed applicant is Sterilization Technical Services, Inc.. It received FDA 510(k) clearance on 1980-11-12 under 510(k) number K802509. The device is classified under product code JTO. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the G.R.A.M. SLIDE?

G.R.A.M. SLIDE is a medical device that received FDA 510(k) clearance on 1980-11-12. The listed applicant is Sterilization Technical Services, Inc.. The 510(k) number is K802509.

When did G.R.A.M. SLIDE receive FDA 510(k) clearance?

G.R.A.M. SLIDE received FDA 510(k) clearance on 1980-11-12, under 510(k) number K802509.

Who is the listed applicant for G.R.A.M. SLIDE?

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

What is the FDA product code for G.R.A.M. SLIDE?

The FDA product code for G.R.A.M. SLIDE is JTO.

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 Sterilization Technical Services, 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.

K812856CHEMICAL INDICATORSK801678SPOR-TEST-STRIP

Related Devices (Code: JTO)

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.

K050352IN-VITRO DIAGNOSTIC VAGINITIS TEST KITAmeritek Research, LLCK970832PYR SWABRemel, Inc.K970834GRAM SWABRemel, Inc.K970833INDOLE SWABRemel, Inc.K970009LYFO(TM) DIFFERENTIAL DISK-BACITRACINMicrobiologics, Inc.K962966IDS RAPID CB PLUS SYSTEMInnovative Diagnostic Systems, 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.

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