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)

ROCHESTER - PEAN FORCEPS, STRAIGHT, 6-1/4+SS

K-Number: K852727 · 1985-07-15

Decision Date1985-07-15
Product CodeHTD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ROCHESTER - PEAN FORCEPS, STRAIGHT, 6-1/4+SS is the device name listed in this FDA 510(k) record. The listed applicant is The Huxley Instrument Corp.. It received FDA 510(k) clearance on 1985-07-15 under 510(k) number K852727. The device is classified under product code HTD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ROCHESTER - PEAN FORCEPS, STRAIGHT, 6-1/4+SS?

ROCHESTER - PEAN FORCEPS, STRAIGHT, 6-1/4+SS is a medical device that received FDA 510(k) clearance on 1985-07-15. The listed applicant is The Huxley Instrument Corp.. The 510(k) number is K852727.

When did ROCHESTER - PEAN FORCEPS, STRAIGHT, 6-1/4+SS receive FDA 510(k) clearance?

ROCHESTER - PEAN FORCEPS, STRAIGHT, 6-1/4+SS received FDA 510(k) clearance on 1985-07-15, under 510(k) number K852727.

Who is the listed applicant for ROCHESTER - PEAN FORCEPS, STRAIGHT, 6-1/4+SS?

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

What is the FDA product code for ROCHESTER - PEAN FORCEPS, STRAIGHT, 6-1/4+SS?

The FDA product code for ROCHESTER - PEAN FORCEPS, STRAIGHT, 6-1/4+SS is HTD.

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 Huxley Instrument 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.

View all 53 devices →

Related Devices (Code: HTD)

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.

↑