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)

INTUBATION PROCEDURE KIT

K-Number: K772046 · 1977-11-23

ApplicantAmerican Hospital Supply Corp.
Decision Date1977-11-23
Product CodeBSR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

INTUBATION PROCEDURE KIT is the device name listed in this FDA 510(k) record. The listed applicant is American Hospital Supply Corp.. It received FDA 510(k) clearance on 1977-11-23 under 510(k) number K772046. The device is classified under product code BSR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTUBATION PROCEDURE KIT?

INTUBATION PROCEDURE KIT is a medical device that received FDA 510(k) clearance on 1977-11-23. The listed applicant is American Hospital Supply Corp.. The 510(k) number is K772046.

When did INTUBATION PROCEDURE KIT receive FDA 510(k) clearance?

INTUBATION PROCEDURE KIT received FDA 510(k) clearance on 1977-11-23, under 510(k) number K772046.

Who is the listed applicant for INTUBATION PROCEDURE KIT?

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

What is the FDA product code for INTUBATION PROCEDURE KIT?

The FDA product code for INTUBATION PROCEDURE KIT is BSR.

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 American Hospital Supply Corp. 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.

K854739AMERICAN STERILE SURGICAL ABSORBENT TOWELK854759AMERICAN STERILE MAYO STAND TRAYK832826AAP DOSIMETRY RELEASE OR BASIN SETSK830546DOSIMETRIC RELEASEK822990CONVERTORS PRIMARY WOUND DRESSING IIK830343CONTAINER W/PRIMING SOLUTION

View all 56 devices →

Related Devices (Code: BSR)

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.

K162729Aintree Intubation Catheter, Arndt Airway Exchange Catheter Set, Cook Airway Exchange Catheter, and Cook Airway Exchange Catheter - Extra Firm With Soft TipCook IncorporatedK962361TRACHLIGHT STYLET AND TRACHEAL LIGHTWANDLaerdal Medical Corp.K954771TRACHLIGHT STYLET & TRACHEAL LIGHTWAND (ORIGINAL APPLICATION NAME: STYLETT & TRACHEAL LIGHTWAND)Laerdal Medical Corp.K943104MOLLOY INTUBATING STYLETTEMolloy Corp.K955238RUSCH SCHROEDER ENDOTRACHEAL TUBE STYLERusch Intl.K953677LIGHTED FLEXGUIDE (MODIFICATION)Scientific Sales Intl., 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.

↑