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)

PROPANE, HIGH PURITY, INSTRUMENT GRADE

K-Number: K770393 · 1977-04-26

ApplicantHycel, Inc.
Decision Date1977-04-26
Product CodeJJO
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

PROPANE, HIGH PURITY, INSTRUMENT GRADE is the device name listed in this FDA 510(k) record. The listed applicant is Hycel, Inc.. It received FDA 510(k) clearance on 1977-04-26 under 510(k) number K770393. The device is classified under product code JJO. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROPANE, HIGH PURITY, INSTRUMENT GRADE?

PROPANE, HIGH PURITY, INSTRUMENT GRADE is a medical device that received FDA 510(k) clearance on 1977-04-26. The listed applicant is Hycel, Inc.. The 510(k) number is K770393.

When did PROPANE, HIGH PURITY, INSTRUMENT GRADE receive FDA 510(k) clearance?

PROPANE, HIGH PURITY, INSTRUMENT GRADE received FDA 510(k) clearance on 1977-04-26, under 510(k) number K770393.

Who is the listed applicant for PROPANE, HIGH PURITY, INSTRUMENT GRADE?

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

What is the FDA product code for PROPANE, HIGH PURITY, INSTRUMENT GRADE?

The FDA product code for PROPANE, HIGH PURITY, INSTRUMENT GRADE is JJO.

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 Hycel, 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.

View all 22 devices →

Related Devices (Code: JJO)

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.

↑