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)

ASEPTIC TRANSFER SET

K-Number: K780417 · 1978-04-18

ApplicantHeyer Schulte Corp.
Decision Date1978-04-18
Product CodeGAZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ASEPTIC TRANSFER SET is the device name listed in this FDA 510(k) record. The listed applicant is Heyer Schulte Corp.. It received FDA 510(k) clearance on 1978-04-18 under 510(k) number K780417. The device is classified under product code GAZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ASEPTIC TRANSFER SET?

ASEPTIC TRANSFER SET is a medical device that received FDA 510(k) clearance on 1978-04-18. The listed applicant is Heyer Schulte Corp.. The 510(k) number is K780417.

When did ASEPTIC TRANSFER SET receive FDA 510(k) clearance?

ASEPTIC TRANSFER SET received FDA 510(k) clearance on 1978-04-18, under 510(k) number K780417.

Who is the listed applicant for ASEPTIC TRANSFER SET?

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

What is the FDA product code for ASEPTIC TRANSFER SET?

The FDA product code for ASEPTIC TRANSFER SET is GAZ.

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 Heyer Schulte 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.

K7920962 FR KELMAN CHAMBER MAINTAINERK790842SUBCUTANEOUS TISSUE EXPANDERK780706LUMBAR NERVE ROOT SHIELDK771224RADOVAN SUBCUTANEOUS TISSUE EXPANDERK760778T-TUBE DRAIN, ROUNDK760784MISHLER 2 CHAMB FLUSHING VALVE,STAND

View all 9 devices →

Related Devices (Code: GAZ)

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.

K952605SUCTION/IRRIGATOR TUBING KITSurgical Laser Technologies, Inc.K945978TUBING, NONINVASIVEEndoscopic Technologies, Inc.K930512SUCTION/IRRIGATION Y TUBING SET W/TRUMPET VALVESCore Dynamics, Inc.K911865NORTEC CONNECTING TUBE SETNorth American Sterilization & Packaging Co.K910471MEDID-VAC CLEAR NONCONDUCTIVE CONNECTING TUBEBaxter Healthcare CorpK910170MAXI-FLOW SUCTION SET 12 FT.Adler Instrument Co.

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.

↑