HS-100 HEADSPACE SAMPLING ACCESSORY
K-Number: K831387 · 1983-08-24
Advertisement
Device Summary
Frequently Asked Questions
What is the HS-100 HEADSPACE SAMPLING ACCESSORY?
HS-100 HEADSPACE SAMPLING ACCESSORY is a medical device that received FDA 510(k) clearance on 1983-08-24. The listed applicant is The Perkin-Elmer Corp.. The 510(k) number is K831387.
When did HS-100 HEADSPACE SAMPLING ACCESSORY receive FDA 510(k) clearance?
HS-100 HEADSPACE SAMPLING ACCESSORY received FDA 510(k) clearance on 1983-08-24, under 510(k) number K831387.
Who is the listed applicant for HS-100 HEADSPACE SAMPLING ACCESSORY?
The FDA 510(k) record lists The Perkin-Elmer Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HS-100 HEADSPACE SAMPLING ACCESSORY?
The FDA product code for HS-100 HEADSPACE SAMPLING ACCESSORY is KZQ.
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.
Other records listing The Perkin-Elmer 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.
Related Devices (Code: KZQ)
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.
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.
Advertisement