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FDA 510(k)

PENTAX FLEXIBLE SIGMOIDOSCOPE MOD. FS-34

K-Number: K792341 · 1979-12-10

ApplicantPentax Precision Instrument Corp.
Decision Date1979-12-10
Product CodeFAM
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PENTAX FLEXIBLE SIGMOIDOSCOPE MOD. FS-34 is the device name listed in this FDA 510(k) record. The listed applicant is Pentax Precision Instrument Corp.. It received FDA 510(k) clearance on 1979-12-10 under 510(k) number K792341. The device is classified under product code FAM. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PENTAX FLEXIBLE SIGMOIDOSCOPE MOD. FS-34?

PENTAX FLEXIBLE SIGMOIDOSCOPE MOD. FS-34 is a medical device that received FDA 510(k) clearance on 1979-12-10. The listed applicant is Pentax Precision Instrument Corp.. The 510(k) number is K792341.

When did PENTAX FLEXIBLE SIGMOIDOSCOPE MOD. FS-34 receive FDA 510(k) clearance?

PENTAX FLEXIBLE SIGMOIDOSCOPE MOD. FS-34 received FDA 510(k) clearance on 1979-12-10, under 510(k) number K792341.

Who is the listed applicant for PENTAX FLEXIBLE SIGMOIDOSCOPE MOD. FS-34?

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

What is the FDA product code for PENTAX FLEXIBLE SIGMOIDOSCOPE MOD. FS-34?

The FDA product code for PENTAX FLEXIBLE SIGMOIDOSCOPE MOD. FS-34 is FAM.

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Other records listing Pentax Precision 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.

K041395EG-3630URK041396FG-36UX FIBER ULTRASOUND GASTROSCOPEK041397EG-3830UTK031789EG-3830UT, VIDEO ULTRASOUND GASTROSCOPEK023401EG-3830UT, VIDEO ULTRASOUND GASTROSCOPEK023376EB-1830T3, VIDEO BRONCHOSCOPE

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Related Devices (Code: FAM)

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.

K964131ENDOSCOPEAkos Biomedical, Inc.K970382VS-100 VIDEO SIGMOIDOSCOPEWelch Allyn, Inc.K964326VISION-SCIENCES MODEL S-V200 COLOR MVIDEO FLEXIBLE SIGMOIDOSCOPE WITH ENDOSHEATH SYSTEMVision-Sciences, Inc.K964100VISION-SCIENCES MODEL SS-U32 ENDO SHEATH FOR USE WITH THE VSI S-F100 FLEXIBLE FIBEROPTIC SIGMOIDOSCOPE AND VSI S-V100Vision-Sciences, Inc.K963344DISPOSABLE SS-F32 ENDOSHEATH FOR USE WITH THE S-F100 FLEXIBLE FIBEROPTIC SIGMOIDOSCOPEVision-Sciences, Inc.K961567ES-3840, VIDEO SIGMOIDOSCOPEPentax Precision Instrument 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.

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