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)

DISPENSING SEROLOGICAL PIPET

K-Number: K801437 · 1980-07-14

ApplicantAmt Corp.
Decision Date1980-07-14
Product CodeJTC
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

DISPENSING SEROLOGICAL PIPET is the device name listed in this FDA 510(k) record. The listed applicant is Amt Corp.. It received FDA 510(k) clearance on 1980-07-14 under 510(k) number K801437. The device is classified under product code JTC. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPENSING SEROLOGICAL PIPET?

DISPENSING SEROLOGICAL PIPET is a medical device that received FDA 510(k) clearance on 1980-07-14. The listed applicant is Amt Corp.. The 510(k) number is K801437.

When did DISPENSING SEROLOGICAL PIPET receive FDA 510(k) clearance?

DISPENSING SEROLOGICAL PIPET received FDA 510(k) clearance on 1980-07-14, under 510(k) number K801437.

Who is the listed applicant for DISPENSING SEROLOGICAL PIPET?

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

What is the FDA product code for DISPENSING SEROLOGICAL PIPET?

The FDA product code for DISPENSING SEROLOGICAL PIPET is JTC.

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

Related Devices (Code: JTC)

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.

K924907FILTERMATE UNIVERSAL HARVESTERPackard Instrument Co., Inc.K901808MICROMATE 196 MODEL A961960Packard Instrument Co., Inc.K894645IMMULON 1,2,3,AND 4 DIVIDASTRIPS TMDynatech Laboratories, Inc.K892369MULTI-PROBE HEAD PLUSHamilton Co.K891766GENETIC SYSTEMS MICROPLATE STRIP WASHERGenetic Systems Corp.K891765GENETIC SYSTEMS PIPETTOR/DILUTORGenetic Systems Corp.

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.

↑